A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892047



Internal ID19186443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85425323..85528944hg38UCSC Ensembl
Outerchr11:85425323..85528944hg38UCSC Ensembl
Innerchr11:85136367..85239988hg19UCSC Ensembl
Outerchr11:85136367..85239988hg19UCSC Ensembl
Innerchr11:84814015..84917636hg18UCSC Ensembl
Outerchr11:84814015..84917636hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38103622
hg19103622
hg18103622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785926
Samples
Known GenesDLG2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892047
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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