A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646104



Internal ID21838151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71537177..71537513hg38UCSC Ensembl
chrX:70757027..70757363hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107842
Supporting Variants
Samples
Known GenesBCYRN1, OGT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646104
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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