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dbVar

Database of genomic structural variation

nsv398046

Organism: Homo sapiens

Study:nstd6 (Mills et al. 2006)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:NCBI35 (hg17)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:9,611

Publication(s):Mills et al. 2006

Links to Other Resources

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: 204 SVs from 30 studies. See in: genome view

Remapped(Score: Perfect):42,182,389-42,191,999

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv398046	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	42,182,389	42,191,999
nsv398046	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	42,039,907	42,049,517
nsv398046	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000008.9	Chr8	42,159,064	42,168,674

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv416624	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv416624	Remapped	Perfect	NC_000008.11:g.421 82389_42191999del9 611	GRCh38.p12	First Pass	NC_000008.11	Chr8	42,182,389	42,191,999
nssv416624	Remapped	Perfect	NC_000008.10:g.420 39907_42049517del9 611	GRCh37.p13	First Pass	NC_000008.10	Chr8	42,039,907	42,049,517
nssv416624	Submitted genomic		NC_000008.9:g.4215 9064_42168674del96 11	NCBI35 (hg17)		NC_000008.9	Chr8	42,159,064	42,168,674

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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