A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515145



Internal ID22573104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:113202020..113214744hg38UCSC Ensembl
chrX:112445247..112457971hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3812725
hg1912725
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977624
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515145
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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