A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177789



Internal ID20744829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57563215..57579870hg38UCSC Ensembl
chr11:57330688..57347343hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3816656
hg1916656
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462996
Supporting Variants
Samples
Known GenesUBE2L6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177789
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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