A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892570



Internal ID19183390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:60832248..60850435hg38UCSC Ensembl
Outerchr2:60832248..60850435hg38UCSC Ensembl
Innerchr2:61059383..61077570hg19UCSC Ensembl
Outerchr2:61059383..61077570hg19UCSC Ensembl
Innerchr2:60912887..60931074hg18UCSC Ensembl
Outerchr2:60912887..60931074hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3818188
hg1918188
hg1818188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782438
Samples
Known GenesFLJ16341
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892570
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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