A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029128



Internal ID18771660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140593589..140635770hg38UCSC Ensembl
Innerchr7:140293389..140335570hg19UCSC Ensembl
Innerchr7:139939858..139982039hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3842182
hg1942182
hg1842182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3664263
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)nsv1029128
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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