A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14268959



Internal ID22204062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:35447105..35470045hg38UCSC Ensembl
OuterchrX:35465222..35488162hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3822941
hg1922941
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197763
Supporting Variants
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14268959
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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