A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893358



Internal ID18837492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63081166..63112536hg38UCSC Ensembl
Outerchr20:63081166..63112536hg38UCSC Ensembl
Innerchr20:61712518..61743888hg19UCSC Ensembl
Outerchr20:61712518..61743888hg19UCSC Ensembl
Innerchr20:61182963..61214333hg18UCSC Ensembl
Outerchr20:61182963..61214333hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3831371
hg1931371
hg1831371
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783895
Samples
Known GenesHAR1A, HAR1B, LOC63930
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893358
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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