A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6642n100



Internal ID20158258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140497279..140535877hg38UCSC Ensembl
chr7:140197079..140235677hg19UCSC Ensembl
chr7:139843548..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 Variants
Supporting Variantsnsv1015856, nsv1019815
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)dgv6642n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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