A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739596



Internal ID163262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21434988..21435039hg38UCSC Ensembl
chrX:21453106..21453157hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562691
Supporting Variants
Samples
Known GenesCNKSR2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739596
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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