A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446825



Internal ID22504695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:131309249..131324361hg38UCSC Ensembl
chrX:130443223..130458335hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg3815113
hg1915113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884122
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446825
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