A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516954



Internal ID22574917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:93610836..93618340hg38UCSC Ensembl
chrX:92865835..92873339hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg387505
hg197505
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970851
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516954
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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