A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739263



Internal ID18366806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:136262309..136267832hg38UCSC Ensembl
Outerchr6:136261081..136269403hg38UCSC Ensembl
Innerchr6:136583447..136588970hg19UCSC Ensembl
Outerchr6:136582219..136590541hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg388323
hg198323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540516
Supporting Variants
Samples
Known GenesBCLAF1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739263
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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