A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892526



Internal ID19183346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:57593810..57617881hg38UCSC Ensembl
Outerchr2:57593810..57617881hg38UCSC Ensembl
Innerchr2:57820945..57845016hg19UCSC Ensembl
Outerchr2:57820945..57845016hg19UCSC Ensembl
Innerchr2:57674449..57698520hg18UCSC Ensembl
Outerchr2:57674449..57698520hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3824072
hg1924072
hg1824072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797253
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892526
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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