A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450229



Internal ID22508099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:80158333..80158333hg38UCSC Ensembl
chrX:79413832..79413832hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5966472
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450229
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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