A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv923n100



Internal ID22787010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70625308..70665972hg38UCSC Ensembl
chr10:72385064..72425728hg19UCSC Ensembl
chr10:72055070..72095734hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3840665
hg1940665
hg1840665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052240, nsv1038318
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)dgv923n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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