A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736136



Internal ID159802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3817000..3831450hg38UCSC Ensembl
chrX:3735041..3749491hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3814451
hg1914451
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421782
Supporting Variants
Samples
Known GenesLOC389906
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736136
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00129534


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