A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741292



Internal ID164958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:87907901..87913892hg38UCSC Ensembl
chrX:87162901..87168892hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg385992
hg195992
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138221
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741292
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00083316


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