A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559047



Internal ID332093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51387865..51387874hg38UCSC Ensembl
chr3:51425296..51425305hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3810
hg1910
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17734861
Samples
Known GenesMANF
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559047
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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