A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739326



Internal ID18366869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:142768964..142769066hg38UCSC Ensembl
Outerchr6:142768958..142769082hg38UCSC Ensembl
Innerchr6:143090101..143090203hg19UCSC Ensembl
Outerchr6:143090095..143090219hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540579
Supporting Variants
Samples
Known GenesHIVEP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739326
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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