A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3566885



Internal ID18767961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:160180002..160180240hg38UCSC Ensembl
Outerchr5:160179968..160180281hg38UCSC Ensembl
Innerchr5:159607009..159607247hg19UCSC Ensembl
Outerchr5:159606975..159607288hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9765632
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3566885
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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