A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739808



Internal ID163474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26164244..26197744hg38UCSC Ensembl
chrX:26182361..26215861hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3833501
hg1933501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6137917
Supporting Variants
Samples
Known GenesMAGEB6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739808
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000628272


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