A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229915



Internal ID22371610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:53023602..53024872hg38UCSC Ensembl
chr13:53597737..53599007hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg381271
hg191271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14368542
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229915
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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