A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582887



Internal ID20955958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83144392..83145776hg38UCSC Ensembl
chr11:82855434..82856818hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381385
hg191385
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220904
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582887
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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