A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892559



Internal ID19183379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:59943740..59956081hg38UCSC Ensembl
Outerchr2:59943740..59956081hg38UCSC Ensembl
Innerchr2:60170875..60183216hg19UCSC Ensembl
Outerchr2:60170875..60183216hg19UCSC Ensembl
Innerchr2:60024379..60036720hg18UCSC Ensembl
Outerchr2:60024379..60036720hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3812342
hg1912342
hg1812342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781264
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892559
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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