A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976191



Internal ID22751126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153176259..153189074hg38UCSC Ensembl
chrX:152476326..152489143hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3812816
hg1912818
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515669, nssv17515668
Samples
Known GenesMAGEA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976191
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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