A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14268314



Internal ID22258684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:79609301..79694140hg38UCSC Ensembl
OuterchrX:78864798..78949637hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3884840
hg1984840
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3204556
Supporting Variants
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14268314
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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