A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv716n100



Internal ID22786803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42118976..42294568hg38UCSC Ensembl
chr10:42614424..42790016hg19UCSC Ensembl
chr10:41934430..42110022hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg38175593
hg19175593
hg18175593
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038298, nsv1047909, nsv1047813, nsv1049686, nsv1039748
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)dgv716n100
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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