A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3643272



Internal ID18594867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:21527109..21646654hg38UCSC Ensembl
Innerchr7:21566727..21686272hg19UCSC Ensembl
Innerchr7:21533252..21652797hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38119546
hg19119546
hg18119546
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025634
Supporting Variants
Samples
Known GenesDNAH11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3643272
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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