A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788501



Internal ID19176527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3677613..3735456hg38UCSC Ensembl
Innerchr11:3698843..3756686hg19UCSC Ensembl
Innerchr11:3655419..3713262hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3857844
hg1957844
hg1857844
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891910
Supporting Variants
Samples
Known GenesNUP98
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788501
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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