A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786895



Internal ID18833127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:409815..419906hg38UCSC Ensembl
Innerchr11:409815..419906hg19UCSC Ensembl
Innerchr11:399815..409906hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3810092
hg1910092
hg1810092
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891907
Supporting Variants
Samples
Known GenesANO9, SIGIRR
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786895
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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