A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781012



Internal ID19176635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:13121084..13142655hg38UCSC Ensembl
Innerchr5:13121196..13142767hg19UCSC Ensembl
Innerchr5:13174196..13195767hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3821572
hg1921572
hg1821572
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894135
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781012
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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