A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv708n100



Internal ID22786795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36985594..37107580hg38UCSC Ensembl
chr10:37274522..37396508hg19UCSC Ensembl
chr10:37314528..37436514hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38121987
hg19121987
hg18121987
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041146, nsv1054192
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)dgv708n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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