A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892625



Internal ID19183445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:70569125..70588059hg38UCSC Ensembl
Outerchr2:70569125..70588059hg38UCSC Ensembl
Innerchr2:70796257..70815191hg19UCSC Ensembl
Outerchr2:70796257..70815191hg19UCSC Ensembl
Innerchr2:70649765..70668699hg18UCSC Ensembl
Outerchr2:70649765..70668699hg18UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3818935
hg1918935
hg1818935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786321
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892625
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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