A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739603



Internal ID163269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21718841..21719973hg38UCSC Ensembl
chrX:21736959..21738091hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg381133
hg191133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415141
Supporting Variants
Samples
Known GenesSMPX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739603
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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