A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891559



Internal ID19185955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14541650..14551811hg38UCSC Ensembl
Outerchr2:14541650..14552637hg38UCSC Ensembl
Innerchr2:14681774..14691935hg19UCSC Ensembl
Outerchr2:14681774..14692761hg19UCSC Ensembl
Innerchr2:14599225..14609386hg18UCSC Ensembl
Outerchr2:14599225..14610212hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3810988
hg1910988
hg1810988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779363, essv25779068, essv25796965, essv25779323, essv25797761, essv25801079, essv25796362, essv25800312
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891559
Frequency
Sample Size3017
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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