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dbVar

Database of genomic structural variation

nsv437777

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:76,393

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: 636 SVs from 83 studies. See in: genome view

Remapped(Score: Perfect):131,411,039-131,487,431

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
nsv437777	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000012.12	Chr12	131,411,039	131,415,578	131,461,962	131,487,431
nsv437777	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	131,895,584	131,900,123	131,946,507	131,971,976
nsv437777	Submitted genomic		NCBI34 (hg16)	Primary Assembly		NC_000012.8	Chr12	130,248,683	130,253,222	130,299,606	130,325,075

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
nssv467658	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
nssv467658	Remapped	Perfect	NC_000012.12:g.(13 1411039_131415578) _(131461962_131487 431)del	GRCh38.p12	First Pass	NC_000012.12	Chr12	131,411,039	131,415,578	131,461,962	131,487,431
nssv467658	Remapped	Perfect	NC_000012.11:g.(13 1895584_131900123) _(131946507_131971 976)del	GRCh37.p13	First Pass	NC_000012.11	Chr12	131,895,584	131,900,123	131,946,507	131,971,976
nssv467658	Submitted genomic		NC_000012.8:g.(130 248683_130253222)_ (130299606_1303250 75)del	NCBI34 (hg16)		NC_000012.8	Chr12	130,248,683	130,253,222	130,299,606	130,325,075

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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