A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225961



Internal ID22368933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66113096..66113259hg38UCSC Ensembl
chr13:66687228..66687391hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14369069, nssv14369070
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225961
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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