A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757134



Internal ID20532994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:134788055..134788055hg38UCSC Ensembl
chrX:133922085..133922085hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275166
Samples
Known GenesFAM122B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757134
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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