A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589958



Internal ID20963029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111715964..111716377hg38UCSC Ensembl
chr11:111586688..111587101hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234292
Samples
Known GenesSIK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589958
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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