A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787675



Internal ID19181470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:106077397..106233242hg38UCSC Ensembl
Innerchr5:105413098..105568943hg19UCSC Ensembl
Innerchr5:105440997..105596842hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38155846
hg19155846
hg18155846
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890701
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787675
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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