A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14387769



Internal ID22273802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49652608..49652608hg38UCSC Ensembl
chr15:49944805..49944805hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3560454
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14387769
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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