A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021133



Internal ID18763667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140570997..140638853hg38UCSC Ensembl
Innerchr7:140270797..140338653hg19UCSC Ensembl
Innerchr7:139917266..139985122hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3867857
hg1967857
hg1867857
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3664261, nssv3664262, nssv3664260
Samples
Known GenesDENND2A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021133
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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