A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637474



Internal ID7024266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100317437..100437921hg38UCSC Ensembl
chr15:100857642..100978126hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38120485
hg19120485
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15350841, essv15350842, essv15350840, essv15350843
SamplesNA20861, HG03914, HG03991, HG04093
Known GenesADAMTS17, CERS3, SPATA41
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637474
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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