A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543423



Internal ID20916671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150424293..150425596hg38UCSC Ensembl
chr1:150396769..150398072hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381304
hg191304
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247522
Samples
Known GenesRPRD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543423
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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