A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14381176



Internal ID22234561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62893488..62893488hg38UCSC Ensembl
chr15:63185687..63185687hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3560718
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14381176
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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