A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780132



Internal ID19173214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:155982520..156244255hg38UCSC Ensembl
Innerchr5:155409530..155671265hg19UCSC Ensembl
Innerchr5:155342108..155603843hg18UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38261736
hg19261736
hg18261736
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890759
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=40
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780132
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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