A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109549



Internal ID22018782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:931216..1197380hg38UCSC Ensembl
chrX:891951..1315497hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38266165
hg19423547
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644338
Samples
Known GenesCRLF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109549
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