A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15350837



Internal ID4491380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100311230..100508356hg38UCSC Ensembl
chr15:100851435..101048561hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38197127
hg19197127
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637473
Supporting Variants
SamplesHG03991
Known GenesADAMTS17, CERS3, SPATA41
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15350837
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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