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dbVar

Database of genomic structural variation

nsv437544

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:65,139

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: 220 SVs from 40 studies. See in: genome view

Remapped(Score: Perfect):37,023,952-37,089,090

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
nsv437544	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	37,023,952	37,033,832	37,068,499	37,089,090
nsv437544	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	37,063,557	37,073,437	37,108,104	37,128,695
nsv437544	Submitted genomic		NCBI34 (hg16)	Primary Assembly		NC_000007.10	Chr7	36,804,704	36,814,584	36,849,251	36,869,842

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
nssv467425	copy number loss	NA19142	SNP array	SNP genotyping analysis	Heterozygous	20

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv467425	Remapped	Perfect	NC_000007.14:g.(37 023952_37033832)_( 37068499_37089090) del	GRCh38.p12	First Pass	NC_000007.14	Chr7	37,023,952	37,033,832	37,068,499	37,089,090
nssv467425	Remapped	Perfect	NC_000007.13:g.(37 063557_37073437)_( 37108104_37128695) del	GRCh37.p13	First Pass	NC_000007.13	Chr7	37,063,557	37,073,437	37,108,104	37,128,695
nssv467425	Submitted genomic		NC_000007.10:g.(36 804704_36814584)_( 36849251_36869842) del	NCBI34 (hg16)		NC_000007.10	Chr7	36,804,704	36,814,584	36,849,251	36,869,842

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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