A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697569



Internal ID15434221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148442307..148459411hg38UCSC Ensembl
Innerchr7:148139399..148156503hg19UCSC Ensembl
Innerchr7:147770332..147787436hg18UCSC Ensembl
Innerchr7:147577047..147594151hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3817105
hg1917105
hg1817105
hg1717105
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520711
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697569
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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