A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515313



Internal ID22573273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:126726130..126735878hg38UCSC Ensembl
chrX:125860113..125869861hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg389749
hg199749
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5972957
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515313
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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