A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205422



Internal ID22354112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:135802788..135892493hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3889706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10302n152
Supporting Variantsnssv14269827, nssv14269826, nssv14269825
SamplesHG00512, HG00733, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205422
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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