A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585769



Internal ID20958840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32022885..32024825hg38UCSC Ensembl
chr11:32044431..32046371hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381941
hg191941
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226401
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585769
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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