A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6431n100



Internal ID22792518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:62904802..63419173hg38UCSC Ensembl
chr7:62365180..62879551hg19UCSC Ensembl
chr7:62002615..62516986hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38514372
hg19514372
hg18514372
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025153, nsv1015861
Samples
Known GenesLOC100287704, LOC100287834, ZNF733P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6431n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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