A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698940



Internal ID15088906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:37397372..37398993hg38UCSC Ensembl
Innerchr7:37436975..37438596hg19UCSC Ensembl
Innerchr7:37403500..37405121hg18UCSC Ensembl
Innerchr7:37210215..37211836hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381622
hg191622
hg181622
hg171622
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523218
Supporting Variants
Samples
Known GenesELMO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698940
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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