A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515203



Internal ID22573162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:116940526..116953505hg38UCSC Ensembl
chrX:116074494..116087473hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3812980
hg1912980
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978937
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515203
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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