A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645283



Internal ID21837330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151916013..151916098hg38UCSC Ensembl
chrX:151084485..151084570hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106584
Supporting Variants
Samples
Known GenesMAGEA4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645283
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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