A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210932



Internal ID22358660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:135575576..135590764hg38UCSC Ensembl
Outerchr7:135260324..135275512hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3815189
hg1915189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14278782
SamplesNA19239
Known GenesNUP205
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210932
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