A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516012



Internal ID22573974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24467388..24548015hg38UCSC Ensembl
chrX:24485505..24566132hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3880628
hg1980628
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967710
Supporting Variants
Samples
Known GenesPDK3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516012
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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