A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693176



Internal ID15083142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88954166..88966337hg38UCSC Ensembl
Innerchr7:88583480..88595651hg19UCSC Ensembl
Innerchr7:88421416..88433587hg18UCSC Ensembl
Innerchr7:88228131..88240302hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3812172
hg1912172
hg1812172
hg1712172
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515995
Supporting Variants
Samples
Known GenesZNF804B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693176
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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