A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892707



Internal ID19183527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:61882935..61991902hg38UCSC Ensembl
Outerchr15:61882935..61991902hg38UCSC Ensembl
Innerchr15:62175134..62284101hg19UCSC Ensembl
Outerchr15:62175134..62284101hg19UCSC Ensembl
Innerchr15:59962426..60071393hg18UCSC Ensembl
Outerchr15:59962426..60071393hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38108968
hg19108968
hg18108968
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780578
Samples
Known GenesVPS13C
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892707
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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