A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015856



Internal ID18758390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140497279..140535877hg38UCSC Ensembl
Innerchr7:140197079..140235677hg19UCSC Ensembl
Innerchr7:139843548..139882146hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3838599
hg1938599
hg1838599
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6642n100
Supporting Variantsnssv3664256
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)nsv1015856
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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