A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17642115



Internal ID21834162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54117353..54117416hg38UCSC Ensembl
chrX:54143786..54143849hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108590
Supporting Variants
Samples
Known GenesFAM120C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17642115
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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