A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559879



Internal ID332899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64077767..64255689hg38UCSC Ensembl
chr2:64304901..64482823hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38177923
hg19177923
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725893
Samples
Known GenesLINC00309, PELI1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559879
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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