A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9766121



Internal ID18740367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:19764972..19770875hg38UCSC Ensembl
Outerchr6:19764775..19771122hg38UCSC Ensembl
Innerchr6:19765203..19771106hg19UCSC Ensembl
Outerchr6:19765006..19771353hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386348
hg196348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3567374
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9766121
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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