A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780727



Internal ID19166283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58047257..58106403hg38UCSC Ensembl
Innerchr15:58339455..58398602hg19UCSC Ensembl
Innerchr15:56126747..56185894hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3859147
hg1959148
hg1859148
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892701
Supporting Variants
Samples
Known GenesALDH1A2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=27
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780727
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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