A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593372



Internal ID20966443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:48355850..48978825hg38UCSC Ensembl
chr11:48377402..49000377hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38622976
hg19622976
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236266
Samples
Known GenesOR4A47
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593372
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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