A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529930



Internal ID22399321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45287803..45287863hg38UCSC Ensembl
chr13:45861938..45861998hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14367596, nssv14367595
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529930
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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