A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586197



Internal ID20959268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57831093..57831591hg38UCSC Ensembl
chr11:57598565..57599063hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38499
hg19499
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586197
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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