A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431481



Internal ID22489351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101800345..101812814hg38UCSC Ensembl
chrX:101055318..101067787hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3812470
hg1912470
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869401
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431481
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003


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