A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv869n100



Internal ID22786956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:56566705..56725241hg38UCSC Ensembl
chr10:58326465..58485001hg19UCSC Ensembl
chr10:57996471..58155007hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38158537
hg19158537
hg18158537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045015, nsv1047489, nsv1054652, nsv1054062, nsv1037340, nsv1047726, nsv1054588, nsv1036583, nsv1037820, nsv1043534, nsv1045583
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)dgv869n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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