A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739386



Internal ID18713632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:151164768..151165658hg38UCSC Ensembl
Outerchr6:151164717..151165882hg38UCSC Ensembl
Innerchr6:151485903..151486793hg19UCSC Ensembl
Outerchr6:151485852..151487017hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381166
hg191166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540639
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739386
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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