A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576269



Internal ID20949340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9994755..9995932hg38UCSC Ensembl
chr11:10016302..10017479hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381178
hg191178
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222733
Samples
Known GenesSBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576269
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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