A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202666



Internal ID22351795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:100222933..100259314hg38UCSC Ensembl
Outerchr4:101144090..101180471hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3836382
hg1936382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14272979
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202666
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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