A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515594



Internal ID22573556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:146532192..146539355hg38UCSC Ensembl
chrX:145613710..145620873hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg387164
hg197164
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973888
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515594
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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