A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14268316



Internal ID22263661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:81813579..81841478hg38UCSC Ensembl
OuterchrX:81069078..81096977hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3827900
hg1927900
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3195113
Supporting Variants
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14268316
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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