A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581541



Internal ID20954612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120869690..120892100hg38UCSC Ensembl
chr11:120740399..120762809hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3822411
hg1922411
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229669
Samples
Known GenesGRIK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581541
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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