A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229129



Internal ID22371074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59980068..59980180hg38UCSC Ensembl
chr15:60272267..60272379hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14376074, nssv14382662
SamplesHG00731, HG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229129
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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