A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697314



Internal ID15433966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85375943..85426350hg38UCSC Ensembl
Innerchr7:85005259..85055666hg19UCSC Ensembl
Innerchr7:84843195..84893602hg18UCSC Ensembl
Innerchr7:84649910..84700317hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3850408
hg1950408
hg1850408
hg1750408
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520264
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697314
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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