A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv921n100



Internal ID22787008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69748668..69775350hg38UCSC Ensembl
chr10:71508424..71535106hg19UCSC Ensembl
chr10:71178430..71205112hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3826683
hg1926683
hg1826683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044630, nsv1038197
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)dgv921n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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