A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562691



Internal ID335636
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 StatusM
Merged Variants
Supporting Variantsnssv17739596
Samples
Known GenesCNKSR2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562691
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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