A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528290



Internal ID22397676
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14387887, nssv14387545, nssv14381595, nssv14388243
SamplesNA19238, NA19239, HG00731, NA19240
Known GenesATP8B4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528290
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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