A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516923



Internal ID22574886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:89902969..89914861hg38UCSC Ensembl
chrX:89157968..89169860hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3811893
hg1911893
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973577
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516923
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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