A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593429



Internal ID20966500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65197836..65198425hg38UCSC Ensembl
chr11:64965307..64965896hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38590
hg19590
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228187
Samples
Known GenesCAPN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593429
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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