A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108944



Internal ID22018177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26194105..26194233hg38UCSC Ensembl
chrX:26212222..26212350hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639525
Samples
Known GenesMAGEB6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108944
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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