A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547518



Internal ID20920719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58312436..58312829hg38UCSC Ensembl
chr3:58298163..58298556hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38394
hg19394
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261579
Samples
Known GenesRPP14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547518
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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