A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185965



Internal ID20753005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61435852..61458449hg38UCSC Ensembl
chr11:61203324..61225921hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3822598
hg1922598
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465044
Supporting Variants
Samples
Known GenesSDHAF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185965
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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