A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738014



Internal ID161680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152127134..152129140hg38UCSC Ensembl
chrX:151295606..151297612hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg382007
hg192007
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427348
Supporting Variants
Samples
Known GenesMAGEA10-MAGEA5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738014
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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