A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv694n100



Internal ID22786781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26601481..26682950hg38UCSC Ensembl
chr10:26890410..26971879hg19UCSC Ensembl
chr10:26930416..27011885hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3881470
hg1981470
hg1881470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044057, nsv1046911, nsv1052412, nsv1041766, nsv1044848
Samples
Known GenesLINC00202-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv694n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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