A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199413



Internal ID22348999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:181546400..181560108hg38UCSC Ensembl
Outerchr4:182467553..182481261hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3813709
hg1913709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14273796
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199413
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