A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058515



Internal ID21967748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22412627..22412627hg38UCSC Ensembl
chrX:22430744..22430744hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638128
Samples
Known GenesLOC100873065
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058515
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer