A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469148



Internal ID22527039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:88985811..88987767hg38UCSC Ensembl
chrX:88240812..88242768hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg381957
hg191957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869484
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469148
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