A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891908



Internal ID18839618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3220993..3381247hg38UCSC Ensembl
Outerchr11:3220993..3381247hg38UCSC Ensembl
Innerchr11:3242223..3402477hg19UCSC Ensembl
Outerchr11:3242223..3402477hg19UCSC Ensembl
Innerchr11:3198799..3359053hg18UCSC Ensembl
Outerchr11:3198799..3359053hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38160255
hg19160255
hg18160255
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781552
Samples
Known GenesLOC650368, MRGPRE, MRGPRG-AS1, ZNF195
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891908
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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