A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv667n100



Internal ID22786754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6609465..6622533hg38UCSC Ensembl
chr10:6651427..6664495hg19UCSC Ensembl
chr10:6691433..6704501hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3813069
hg1913069
hg1813069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047226, nsv1055086
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)dgv667n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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