A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557339



Internal ID330438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33412268..33823627hg38UCSC Ensembl
chr9:33412266..33823625hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38411360
hg19411360
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023521
Samples
Known GenesANKRD18B, ANXA2P2, AQP3, LOC101929688, MIR6851, NOL6, PRSS3, PTENP1, PTENP1-AS, SUGT1P1, UBE2R2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557339
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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