A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560718



Internal ID22429515
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14383276, nssv14381176
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560718
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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