A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6761n100



Internal ID20158377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:153235178..153829191hg38UCSC Ensembl
chr7:152932263..153526276hg19UCSC Ensembl
chr7:152563196..153157209hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38594014
hg19594014
hg18594014
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028109, nsv1034277, nsv1023927
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6761n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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