A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655629



Internal ID18953910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:67179505..67320042hg38UCSC Ensembl
Innerchr7:66644492..66785029hg19UCSC Ensembl
Innerchr7:66281927..66422464hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38140538
hg19140538
hg18140538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032237
Supporting Variants
Samples
Known GenesPMS2P4, STAG3L4, TYW1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655629
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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