A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516690



Internal ID22574653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71321476..71328771hg38UCSC Ensembl
chrX:70541326..70548621hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg387296
hg197296
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974408
Supporting Variants
Samples
Known GenesBCYRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516690
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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