A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467976



Internal ID22525865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:88472485..88731230hg38UCSC Ensembl
chrX:87727486..87986231hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38258746
hg19258746
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885527
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467976
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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