A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567701



Internal ID18768777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:41953127..41954349hg38UCSC Ensembl
Outerchr6:41953087..41954455hg38UCSC Ensembl
Innerchr6:41920865..41922087hg19UCSC Ensembl
Outerchr6:41920825..41922193hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381369
hg191369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9766448
Samples
Known GenesCCND3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567701
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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