A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594284



Internal ID20967355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58701410..58702341hg38UCSC Ensembl
chr11:58468883..58469814hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38932
hg19932
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1182n223
Supporting Variantsnssv18226344
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594284
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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