A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515645



Internal ID22573607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152834834..152883858hg38UCSC Ensembl
chrX:152003378..152052402hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3849025
hg1949025
Variant TypeOTHER copy number variation
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973043
Supporting Variants
Samples
Known GenesNSDHL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515645
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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