A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441281



Internal ID22499151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:14084..226386hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38212303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872001
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441281
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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