A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5549293



Internal ID322971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101759567..101759569hg38UCSC Ensembl
chr12:102153345..102153347hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17690379
Samples
Known GenesGNPTAB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5549293
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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