A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14350679



Internal ID22207254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23912222..23912525hg38UCSC Ensembl
chrX:23930339..23930642hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3202071
Supporting Variants
SamplesHG00732
Known GenesCXorf58
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14350679
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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