A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201322



Internal ID22350652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:154590912..154613506hg38UCSC Ensembl
OuterchrX:153819175..153841759hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3822595
hg1922585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14269264
SamplesNA19239
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201322
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