A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17647990



Internal ID21840037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:100555159..100730317hg38UCSC Ensembl
chrX:99810156..99985305hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38175159
hg19175150
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105116
Supporting Variants
Samples
Known GenesSRPX2, SYTL4, TNMD, TSPAN6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17647990
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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