A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427348



Internal ID206253
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 StatusM
Merged Variants
Supporting Variantsnssv17738014
Samples
Known GenesMAGEA10-MAGEA5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427348
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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