A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10862n54



Internal ID22778757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:100532998..100637070hg38UCSC Ensembl
chr6:100980874..101084946hg19UCSC Ensembl
chr6:101087595..101191667hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38104073
hg19104073
hg18104073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604263, nsv604264
Samples
Known GenesASCC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10862n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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