A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678359



Internal ID15415011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38329947..38333930hg38UCSC Ensembl
Innerchr7:38369548..38373531hg19UCSC Ensembl
Innerchr7:38336073..38340056hg18UCSC Ensembl
Innerchr7:38142788..38146771hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg383984
hg193984
hg183984
hg173984
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519863
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678359
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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