A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9752158



Internal ID18726404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:20466921..20467200hg38UCSC Ensembl
Outerchr2:20466852..20467277hg38UCSC Ensembl
Innerchr2:20666682..20666961hg19UCSC Ensembl
Outerchr2:20666613..20667038hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38426
hg19426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3553411
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9752158
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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