A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14377749



Internal ID22167309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81246136..81246859hg38UCSC Ensembl
chr15:81538477..81539200hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3229818
Supporting Variants
SamplesHG00514
Known GenesIL16
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14377749
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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