A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439454



Internal ID22497324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:116327424..116427380hg38UCSC Ensembl
chrX:115458559..115558542hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3899957
hg1999984
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5886988
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439454
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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