A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736473



Internal ID160139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:39538100..39538104hg38UCSC Ensembl
chrX:39397354..39397358hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5551881
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736473
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.012176


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