A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876917



Internal ID22651879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:130989174..130989225hg38UCSC Ensembl
chrX:130123148..130123199hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446206
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876917
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