A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14392069



Internal ID22289089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41031621..41040138hg38UCSC Ensembl
chr15:41323819..41332336hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg388518
hg198518
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220960
Supporting Variants
SamplesNA19240
Known GenesINO80
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14392069
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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