A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736421



Internal ID160087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37691831..37692113hg38UCSC Ensembl
chrX:37551084..37551366hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428604
Supporting Variants
Samples
Known GenesXK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736421
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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