A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559923



Internal ID22428718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101334388..101334388hg38UCSC Ensembl
chr13:101986739..101986739hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14369755
SamplesNA19240
Known GenesNALCN
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559923
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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