A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739339



Internal ID18713585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:145384502..145385377hg38UCSC Ensembl
Outerchr6:145384303..145385475hg38UCSC Ensembl
Innerchr6:145705638..145706513hg19UCSC Ensembl
Outerchr6:145705439..145706611hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg381173
hg191173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540592
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739339
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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