A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14350372



Internal ID22230001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41262127..41262244hg38UCSC Ensembl
chrX:41121380..41121497hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3190795
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14350372
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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