A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868832



Internal ID22643767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:65081329..65081409hg38UCSC Ensembl
chrX:64301209..64301289hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461806
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868832
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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