A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529194



Internal ID22398587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51407898..51408301hg38UCSC Ensembl
chr13:51982034..51982437hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14368474, nssv14368475
SamplesNA19240, HG00733
Known GenesINTS6
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529194
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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