A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5534964



Internal ID310683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12124877..12124928hg38UCSC Ensembl
chr1:12184934..12184985hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16894186
Samples
Known GenesTNFRSF8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5534964
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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