A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352833



Internal ID22280557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:90323367..90325381hg38UCSC Ensembl
chrX:89578366..89580380hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg382015
hg192015
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3204437
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352833
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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