A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14353181



Internal ID22233349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:104853626..104853920hg38UCSC Ensembl
chrX:104098306..104098600hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197632
Supporting Variants
SamplesHG00733
Known GenesIL1RAPL2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14353181
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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