A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572834



Internal ID20945905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111006091..111007955hg38UCSC Ensembl
chr6:111327294..111329158hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381865
hg191865
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268471
Samples
Known GenesRPF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572834
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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