A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563882



Internal ID22432618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173765944..173765944hg38UCSC Ensembl
chr5:173192947..173192947hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14324557, nssv14324554, nssv14324558, nssv14324556, nssv14324559, nssv14324555
SamplesHG00512, HG00731, HG00732, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563882
Frequency
Sample Size9
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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