A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655177



Internal ID18953458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85550202..85609829hg38UCSC Ensembl
Innerchr7:85179518..85239145hg19UCSC Ensembl
Innerchr7:85017454..85077081hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3859628
hg1959628
hg1859628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021978
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655177
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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