A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109905



Internal ID22019138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:39858258..39871448hg38UCSC Ensembl
chrX:39717512..39730702hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3813191
hg1913191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640393
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109905
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