A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586269



Internal ID20959340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45752958..45753105hg38UCSC Ensembl
chr11:45774509..45774656hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234832
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586269
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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