A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207775



Internal ID22356115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:29742496..29793579hg38UCSC Ensembl
Outerchr3:29783987..29835070hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3851084
hg1951084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14271116
SamplesHG00513
Known GenesRBMS3
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207775
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