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dbVar

Database of genomic structural variation

nsv834137

Organism: Homo sapiens

Study:nstd68 (Wong et al. 2006)
Variant Type:copy number variation
Method Type:BAC aCGH
Submitted on:NCBI35 (hg17)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:230,250

Publication(s):Wong et al. 2006

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: 739 SVs from 72 studies. See in: genome view

Remapped(Score: Perfect):57,456,514-57,686,763

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv834137	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	57,456,514	57,686,763
nsv834137	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	57,683,649	57,913,898
nsv834137	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000002.9	Chr2	57,595,300	57,825,549

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv1441924	copy number gain	BAC aCGH	Probe signal intensity

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nssv1441924	Remapped	Perfect	NC_000002.12:g.(57 456514_?)_(?_57686 763)dup	GRCh38.p12	First Pass	NC_000002.12	Chr2	57,456,514	57,686,763
nssv1441924	Remapped	Perfect	NC_000002.11:g.(57 683649_?)_(?_57913 898)dup	GRCh37.p13	First Pass	NC_000002.11	Chr2	57,683,649	57,913,898
nssv1441924	Submitted genomic		NC_000002.9:g.(575 95300_?)_(?_578255 49)dup	NCBI35 (hg17)		NC_000002.9	Chr2	57,595,300	57,825,549

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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