A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661490



Internal ID18959771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:57220433..57960277hg38UCSC Ensembl
Innerchr7:57288140..58019983hg19UCSC Ensembl
Innerchr7:57292082..58023925hg18UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38739845
hg19731844
hg18731844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030441
Supporting Variants
Samples
Known GenesMIR3147, ZNF716
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3661490
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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