A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739139



Internal ID18713385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:121995974..121998490hg38UCSC Ensembl
Outerchr6:121995646..121998982hg38UCSC Ensembl
Innerchr6:122317120..122319636hg19UCSC Ensembl
Outerchr6:122316792..122320128hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg383337
hg193337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540392
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739139
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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