A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742765



Internal ID166431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:141903766..141904068hg38UCSC Ensembl
chrX:140991552..140991854hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414680
Supporting Variants
Samples
Known GenesMAGEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742765
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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