A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543443



Internal ID20916691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:211298732..211300065hg38UCSC Ensembl
chr1:211472074..211473407hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg381334
hg191334
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247881
Samples
Known GenesRCOR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543443
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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