A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893601



Internal ID18837735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:62162003..62343094hg38UCSC Ensembl
Outerchr1:62162003..62343094hg38UCSC Ensembl
Innerchr1:62627675..62808765hg19UCSC Ensembl
Outerchr1:62627675..62808765hg19UCSC Ensembl
Innerchr1:62400263..62581353hg18UCSC Ensembl
Outerchr1:62400263..62581353hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38181092
hg19181091
hg18181091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796757
Samples
Known GenesINADL, KANK4, L1TD1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893601
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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