A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785778



Internal ID18831091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:60333980..60349653hg38UCSC Ensembl
Innerchr11:60101453..60117126hg19UCSC Ensembl
Innerchr11:59858029..59873702hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3815674
hg1915674
hg1815674
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892019
Supporting Variants
Samples
Known GenesMS4A6E
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785778
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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