A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10302n152



Internal ID22826005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX: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 Variants
Supporting Variantsnsv3205422, nsv3196506
SamplesHG00512, NA19239, NA19240, HG00733, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv10302n152
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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