A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351113



Internal ID22207478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47090909..47090961hg38UCSC Ensembl
chrX:46950308..46950360hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3208811
Supporting Variants
SamplesHG00732
Known GenesRGN
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351113
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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