A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351096



Internal ID22231130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45940549..45940601hg38UCSC Ensembl
chrX:45799984..45800036hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3191436
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351096
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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