A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033685



Internal ID18776218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140497279..140524503hg38UCSC Ensembl
Innerchr7:140197079..140224303hg19UCSC Ensembl
Innerchr7:139843548..139870772hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3827225
hg1927225
hg1827225
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3664255
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)nsv1033685
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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