A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516359



Internal ID22574322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52862005..52876733hg38UCSC Ensembl
chrX:52891034..52905764hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3814729
hg1914731
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971180
Supporting Variants
Samples
Known GenesXAGE3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516359
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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