A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967746



Internal ID22742682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9417602..9422237hg38UCSC Ensembl
chrX:9385642..9390277hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg384636
hg194636
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516961
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967746
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