A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515417



Internal ID22573378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:13462832..13485409hg38UCSC Ensembl
chrX:13480951..13503528hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3822578
hg1922578
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979858
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515417
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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