A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179442



Internal ID20746482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62587509..62592164hg38UCSC Ensembl
chr11:62354981..62359636hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg384656
hg194656
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457270
Supporting Variants
Samples
Known GenesTUT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179442
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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