A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796621



Internal ID19168314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:81163627..81171978hg38UCSC Ensembl
Innerchr5:80459446..80467797hg19UCSC Ensembl
Innerchr5:80495202..80503553hg18UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg388352
hg198352
hg188352
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890663
Supporting Variants
Samples
Known GenesRASGRF2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796621
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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