A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875371



Internal ID22650328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37842388..37842438hg38UCSC Ensembl
chrX:37701641..37701691hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459078
Samples
Known GenesDYNLT3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875371
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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