A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561136



Internal ID22429928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79652543..79652543hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3857
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282524, nssv14282523, nssv14282525
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561136
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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