A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739181



Internal ID18713427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:125387740..125390045hg38UCSC Ensembl
Outerchr6:125387521..125390291hg38UCSC Ensembl
Innerchr6:125708886..125711191hg19UCSC Ensembl
Outerchr6:125708667..125711437hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg382771
hg192771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540434
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739181
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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