A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593734



Internal ID20966805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76365151..76365637hg38UCSC Ensembl
chr11:76076195..76076681hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38487
hg19487
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236174
Samples
Known GenesPRKRIR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593734
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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