A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3203867



Internal ID22352811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:5124754..5198347hg38UCSC Ensembl
OuterchrX:5042795..5116388hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3873594
hg1973594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10015n152
Supporting Variantsnssv14270667
SamplesNA19239
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3203867
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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