A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516988



Internal ID22574951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:97351379..97353739hg38UCSC Ensembl
chrX:96606378..96608738hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg382361
hg192361
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5969154
Supporting Variants
Samples
Known GenesDIAPH2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516988
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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