A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545000



Internal ID20918237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:6297812..8759871hg38UCSC Ensembl
chr3:6339499..8801557hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg382462060
hg192462059
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262248
Samples
Known GenesCAV3, GRM7, LINC00312, LMCD1, LMCD1-AS1, OXTR, SSUH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545000
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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