A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973480



Internal ID22748415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27809292..27816761hg38UCSC Ensembl
chrX:27827409..27834878hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg387470
hg197470
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516070
Samples
Known GenesMAGEB10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973480
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