A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17643369



Internal ID21835416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152120472..152120529hg38UCSC Ensembl
chrX:151288944..151289001hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112585
Supporting Variants
Samples
Known GenesMAGEA10-MAGEA5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17643369
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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