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dbVar

Database of genomic structural variation

nsv483115

Organism: Homo sapiens

Study:nstd41 (Iafrate et al. 2004)
Variant Type:copy number variation
Method Type:BAC aCGH
Submitted on:GRCh37 (hg19)

Variant Calls:5
Validation:Not tested
Clinical Assertions: No
Region Size:164,346

Publication(s):Iafrate et al. 2004

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 736 SVs from 70 studies. See in: genome view

Remapped(Score: Perfect):170,202,461-170,366,806

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv483115	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	170,202,461	170,366,806
nsv483115	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	171,123,612	171,287,957

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv2996064	copy number gain	BAC aCGH	Probe signal intensity
nssv2996200	copy number gain	BAC aCGH	Probe signal intensity
nssv2996256	copy number gain	BAC aCGH	Probe signal intensity
nssv2996320	copy number gain	BAC aCGH	Probe signal intensity
nssv2996544	copy number gain	BAC aCGH	Probe signal intensity

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv2996064	Remapped	Perfect	NC_000004.12:g.(?_ 170202461)_(170366 806_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	170,202,461	170,366,806
nssv2996200	Remapped	Perfect	NC_000004.12:g.(?_ 170202461)_(170366 806_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	170,202,461	170,366,806
nssv2996256	Remapped	Perfect	NC_000004.12:g.(?_ 170202461)_(170366 806_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	170,202,461	170,366,806
nssv2996320	Remapped	Perfect	NC_000004.12:g.(?_ 170202461)_(170366 806_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	170,202,461	170,366,806
nssv2996544	Remapped	Perfect	NC_000004.12:g.(?_ 170202461)_(170366 806_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	170,202,461	170,366,806
nssv2996064	Submitted genomic		NC_000004.11:g.(?_ 171123612)_(171287 957_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	171,123,612	171,287,957
nssv2996200	Submitted genomic		NC_000004.11:g.(?_ 171123612)_(171287 957_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	171,123,612	171,287,957
nssv2996256	Submitted genomic		NC_000004.11:g.(?_ 171123612)_(171287 957_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	171,123,612	171,287,957
nssv2996320	Submitted genomic		NC_000004.11:g.(?_ 171123612)_(171287 957_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	171,123,612	171,287,957
nssv2996544	Submitted genomic		NC_000004.11:g.(?_ 171123612)_(171287 957_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	171,123,612	171,287,957

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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