A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567580



Internal ID18421970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32827730..32827897hg38UCSC Ensembl
Outerchr6:32827701..32827921hg38UCSC Ensembl
Innerchr6:32795507..32795674hg19UCSC Ensembl
Outerchr6:32795478..32795698hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9766327
Samples
Known GenesTAP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567580
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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