A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14268855



Internal ID22121964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:42651738..42673240hg38UCSC Ensembl
OuterchrX:42510990..42532491hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3821503
hg1921502
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3199384
Supporting Variants
SamplesHG00512
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14268855
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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