A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701649



Internal ID15091615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:37334906..37339971hg38UCSC Ensembl
Innerchr7:37374510..37379575hg19UCSC Ensembl
Innerchr7:37341035..37346100hg18UCSC Ensembl
Innerchr7:37147750..37152815hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg385066
hg195066
hg185066
hg175066
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525516
Supporting Variants
Samples
Known GenesELMO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701649
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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