A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892492



Internal ID19183312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:56675574..56703959hg38UCSC Ensembl
Outerchr2:56675574..56703959hg38UCSC Ensembl
Innerchr2:56902709..56931094hg19UCSC Ensembl
Outerchr2:56902709..56931094hg19UCSC Ensembl
Innerchr2:56756213..56784598hg18UCSC Ensembl
Outerchr2:56756213..56784598hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3828386
hg1928386
hg1828386
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800356
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892492
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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