A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584567



Internal ID20957638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112206055..112206121hg38UCSC Ensembl
chr11:112076778..112076844hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234658
Samples
Known GenesBCO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584567
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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