A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202911



Internal ID22352006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:161129268..161175188hg38UCSC Ensembl
Outerchr5:160556275..160602195hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3845921
hg1945921
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14272737, nssv14272739, nssv14272738
SamplesNA19238, HG00731, NA19240
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202911
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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