A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892033



Internal ID19186429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81568307..81612542hg38UCSC Ensembl
Outerchr11:81568307..81612542hg38UCSC Ensembl
Innerchr11:81279349..81323584hg19UCSC Ensembl
Outerchr11:81279349..81323584hg19UCSC Ensembl
Innerchr11:80956997..81001232hg18UCSC Ensembl
Outerchr11:80956997..81001232hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3844236
hg1944236
hg1844236
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781508
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892033
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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