A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799778



Internal ID18813154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34408096..34515668hg38UCSC Ensembl
Innerchr15:34700297..34807869hg19UCSC Ensembl
Innerchr15:32487589..32595161hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38107573
hg19107573
hg18107573
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892664
Supporting Variants
Samples
Known GenesGOLGA8A
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799778
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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