A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955070



Internal ID22730292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:145708477..145708477hg38UCSC Ensembl
chrX:144789995..144789995hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430783
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955070
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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