A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648401



Internal ID21840448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47847991..48395972hg38UCSC Ensembl
chrX:47707390..48255414hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38547982
hg19548025
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108328
Supporting Variants
Samples
Known GenesSPACA5, SPACA5B, SSX1, SSX3, SSX4, SSX4B, SSX5, SSX6, SSX9, ZNF182, ZNF630, ZNF81
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648401
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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