A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567702



Internal ID18768778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:41985525..41988762hg38UCSC Ensembl
Outerchr6:41985263..41989262hg38UCSC Ensembl
Innerchr6:41953263..41956500hg19UCSC Ensembl
Outerchr6:41953001..41957000hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9766449
Samples
Known GenesCCND3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567702
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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