A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445645



Internal ID22503515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120818679..120870295hg38UCSC Ensembl
chrX:119952533..120004149hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3851617
hg1951617
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880670
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445645
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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