A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971725



Internal ID22746660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102799030..102810464hg38UCSC Ensembl
chrX:102053958..102065392hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3811435
hg1911435
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515052
Samples
Known GenesLINC00630
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971725
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