A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562082



Internal ID20935153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112732808..112733484hg38UCSC Ensembl
chr3:112451655..112452331hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562082
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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