A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969501



Internal ID22744436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149808422..149911730hg38UCSC Ensembl
chrX:148890084..149032062hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38103309
hg19141979
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515618
Samples
Known GenesMAGEA8, MAGEA8-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969501
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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