A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018535



Internal ID18761068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140498740..140524503hg38UCSC Ensembl
Innerchr7:140198540..140224303hg19UCSC Ensembl
Innerchr7:139845009..139870772hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3825764
hg1925764
hg1825764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3664258
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)nsv1018535
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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