A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736322



Internal ID159988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:28186218..28310616hg38UCSC Ensembl
chrX:28204335..28328733hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38124399
hg19124399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138128
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736322
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000832813


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