A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893332



Internal ID19184152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:36415386..36446639hg38UCSC Ensembl
Outerchr20:36415386..36446639hg38UCSC Ensembl
Innerchr20:35043789..35075042hg19UCSC Ensembl
Outerchr20:35043789..35075042hg19UCSC Ensembl
Innerchr20:34477203..34508456hg18UCSC Ensembl
Outerchr20:34477203..34508456hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3831254
hg1931254
hg1831254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780763
Samples
Known GenesDLGAP4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893332
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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