A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976573



Internal ID22751508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:147186894..147196029hg38UCSC Ensembl
chrX:146268412..146277547hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg389136
hg199136
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515597
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976573
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