A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220511



Internal ID22365185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98063851..98065700hg38UCSC Ensembl
chr13:98716105..98717954hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg381850
hg191850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2395n152
Supporting Variantsnssv14371764, nssv14369658, nssv14371768, nssv14371765, nssv14371769, nssv14371770, nssv14371766, nssv14369657, nssv14371767
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)nsv3220511
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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