A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736956



Internal ID160622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:51618000..51676964hg38UCSC Ensembl
chrX:51360852..51419897hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3858965
hg1959046
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138367
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736956
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000627484


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