A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515643



Internal ID22573605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152829333..152838355hg38UCSC Ensembl
chrX:151997877..152006899hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg389023
hg199023
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973129
Supporting Variants
Samples
Known GenesCETN2, NSDHL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515643
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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