A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662111



Internal ID18960392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:121178328..121400522hg38UCSC Ensembl
Innerchr7:120818382..121040576hg19UCSC Ensembl
Innerchr7:120605618..120827812hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38222195
hg19222195
hg18222195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034353
Supporting Variants
Samples
Known GenesCPED1, FAM3C, WNT16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3662111
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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