A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3204144



Internal ID22353042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:98335936..98381770hg38UCSC Ensembl
Outerchr5:97671640..97717474hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3845835
hg1945835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14273378
SamplesHG00512
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3204144
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer