A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736197



Internal ID159863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5443766..5445045hg38UCSC Ensembl
chrX:5361807..5363086hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg381280
hg191280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417960
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736197
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.006558


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