A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595423



Internal ID20968494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61443778..61444554hg38UCSC Ensembl
chr11:61211250..61212026hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38777
hg19777
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228785
Samples
Known GenesSDHAF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595423
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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