A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883232



Internal ID22658210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37036094..37048317hg38UCSC Ensembl
chrX:37054167..37066390hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3812224
hg1912224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457554
Samples
Known GenesFTH1P18
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883232
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