A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979164



Internal ID22754099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:97514783..97528013hg38UCSC Ensembl
chrX:96769782..96783012hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3813231
hg1913231
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516991
Samples
Known GenesDIAPH2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979164
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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