A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584103



Internal ID20957174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59130435..59131451hg38UCSC Ensembl
chr11:58897908..58898924hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584103
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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