A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678829



Internal ID15415481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111588117..111689280hg38UCSC Ensembl
Innerchr7:111228173..111329336hg19UCSC Ensembl
Innerchr7:111015409..111116572hg18UCSC Ensembl
Innerchr7:110822124..110923287hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38101164
hg19101164
hg18101164
hg17101164
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517394
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678829
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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