A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737036



Internal ID160702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53472964..53508964hg38UCSC Ensembl
chrX:53499916..53535930hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3836001
hg1936015
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138442
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737036
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000835946


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