A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782443



Internal ID19171606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:97019528..97024683hg38UCSC Ensembl
Innerchr15:97562758..97567913hg19UCSC Ensembl
Innerchr15:95363762..95368917hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg385156
hg195156
hg185156
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892735
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782443
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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