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dbVar

Database of genomic structural variation

nsv437605

Organism: Homo sapiens

Study:nstd17 (Conrad et al. 2005)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:NCBI34 (hg16)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:65,806

Publication(s):Conrad et al. 2005

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: 709 SVs from 75 studies. See in: genome view

Remapped(Score: Good):16,402,657-16,468,462

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nsv437605	Remapped	Good	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	16,402,657	16,402,657	16,468,462	16,468,462
nsv437605	Remapped	Good	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	16,260,166	16,260,166	16,325,971	16,325,971
nsv437605	Submitted genomic		NCBI34 (hg16)	Primary Assembly		NC_000008.8	Chr8	16,270,532	16,275,080	16,284,727	16,336,335

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
nssv467486	copy number loss	NA19205	SNP array	SNP genotyping analysis	Heterozygous	25

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv467486	Remapped	Good	NC_000008.11:g.(16 402657_16402657)_( 16468462_16468462) del	GRCh38.p12	First Pass	NC_000008.11	Chr8	16,402,657	16,402,657	16,468,462	16,468,462
nssv467486	Remapped	Good	NC_000008.10:g.(16 260166_16260166)_( 16325971_16325971) del	GRCh37.p13	First Pass	NC_000008.10	Chr8	16,260,166	16,260,166	16,325,971	16,325,971
nssv467486	Submitted genomic		NC_000008.8:g.(162 70532_16275080)_(1 6284727_16336335)d el	NCBI34 (hg16)		NC_000008.8	Chr8	16,270,532	16,275,080	16,284,727	16,336,335

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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