A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567544



Internal ID18421934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32346021..32346311hg38UCSC Ensembl
Outerchr6:32345953..32346339hg38UCSC Ensembl
Innerchr6:32313798..32314088hg19UCSC Ensembl
Outerchr6:32313730..32314116hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9766291
Samples
Known GenesC6orf10
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567544
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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