A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591536



Internal ID20964607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101491139..101491908hg38UCSC Ensembl
chr11:101361870..101362639hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38770
hg19770
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220053
Samples
Known GenesTRPC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591536
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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