A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14379922



Internal ID22126914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68825360..68825645hg38UCSC Ensembl
chr15:69117699..69117984hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213357
Supporting Variants
SamplesHG00512
Known GenesMIR548H4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14379922
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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