A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559249



Internal ID22428053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16323447..16323447hg38UCSC Ensembl
chr10:16365446..16365446hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14333361, nssv14333364, nssv14333357, nssv14333365, nssv14333359, nssv14333363, nssv14333360, nssv14333358, nssv14333362
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559249
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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