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dbVar

Database of genomic structural variation

nsv398013

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:9,925

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: 218 SVs from 22 studies. See in: genome view

Remapped(Score: Perfect):32,474,675-32,484,599

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv398013	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	32,474,675	32,484,599
nsv398013	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	32,332,191	32,342,115
nsv398013	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000008.9	Chr8	32,451,733	32,461,657

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv416591	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv416591	Remapped	Perfect	NC_000008.11:g.324 74675_32484599del9 925	GRCh38.p12	First Pass	NC_000008.11	Chr8	32,474,675	32,484,599
nssv416591	Remapped	Perfect	NC_000008.10:g.323 32191_32342115del9 925	GRCh37.p13	First Pass	NC_000008.10	Chr8	32,332,191	32,342,115
nssv416591	Submitted genomic		NC_000008.9:g.3245 1733_32461657del99 25	NCBI35 (hg17)		NC_000008.9	Chr8	32,451,733	32,461,657

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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