A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592279



Internal ID20965350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27747099..27748102hg38UCSC Ensembl
chr11:27768646..27769649hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg381004
hg191004
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1012n223
Supporting Variantsnssv18225784
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592279
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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