A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698124



Internal ID15088090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85108367..85109179hg38UCSC Ensembl
Innerchr7:84737683..84738495hg19UCSC Ensembl
Innerchr7:84575619..84576431hg18UCSC Ensembl
Innerchr7:84382334..84383146hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38813
hg19813
hg18813
hg17813
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521507
Supporting Variants
Samples
Known GenesSEMA3D
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698124
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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