A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515652



Internal ID22573614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153063865..153100537hg38UCSC Ensembl
chrX:152232231..152366363hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3836673
hg19134133
Variant TypeOTHER copy number variation
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979789
Supporting Variants
Samples
Known GenesPNMA6A, PNMA6C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515652
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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