A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3566694



Internal ID18767770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:137668875..137669508hg38UCSC Ensembl
Outerchr5:137668864..137669522hg38UCSC Ensembl
Innerchr5:137004564..137005197hg19UCSC Ensembl
Outerchr5:137004553..137005211hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38659
hg19659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9765441
Samples
Known GenesKLHL3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3566694
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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