A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103274



Internal ID22012507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48945489..48945552hg38UCSC Ensembl
chrX:48802749..48802812hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645294
Samples
Known GenesOTUD5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103274
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