A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166519



Internal ID21480687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152751418..152751539hg38UCSC Ensembl
chrX:151919942..151920063hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668969
Supporting Variants
SamplesHG03683
Known GenesMAGEA2, MAGEA2B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166519
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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