A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737025



Internal ID160691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53248084..53248095hg38UCSC Ensembl
chrX:53277266..53277277hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536871
Supporting Variants
Samples
Known GenesIQSEC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737025
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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