A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423122



Internal ID22480992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34095947..34432012hg38UCSC Ensembl
chr3:34137439..34473504hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38336066
hg19336066
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973848
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423122
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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