A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3656491



Internal ID18608086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:73444580..73670500hg38UCSC Ensembl
Innerchr7:72858910..73084830hg19UCSC Ensembl
Innerchr7:72496846..72722766hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38225921
hg19225921
hg18225921
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023520
Supporting Variants
Samples
Known GenesBAZ1B, BCL7B, MLXIPL, TBL2, VPS37D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3656491
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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