A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892698



Internal ID19183518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55957090..55977017hg38UCSC Ensembl
Outerchr15:55957090..55977017hg38UCSC Ensembl
Innerchr15:56249288..56269215hg19UCSC Ensembl
Outerchr15:56249288..56269215hg19UCSC Ensembl
Innerchr15:54036580..54056507hg18UCSC Ensembl
Outerchr15:54036580..54056507hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3819928
hg1919928
hg1819928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786982
Samples
Known GenesNEDD4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892698
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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