A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871583



Internal ID22646521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:58222679..58234035hg38UCSC Ensembl
chrX:58249113..58260469hg19UCSC Ensembl
CytobandXp11.1
Allele length
AssemblyAllele length
hg3811357
hg1911357
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459170
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871583
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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