A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739003



Internal ID162669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2444793..2456605hg38UCSC Ensembl
chrX:2362834..2374646hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3811813
hg1911813
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418136
Supporting Variants
Samples
Known GenesDHRSX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739003
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000833854


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