A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14268935



Internal ID22188280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:88484783..88498246hg38UCSC Ensembl
OuterchrX:87739784..87753247hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3813464
hg1913464
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3191341
Supporting Variants
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14268935
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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