A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14387545



Internal ID22196501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49861025..49861077hg38UCSC Ensembl
chr15:50153222..50153274hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528290
Supporting Variants
SamplesHG00731
Known GenesATP8B4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14387545
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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