A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187875



Internal ID20754915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68635033..68717035hg38UCSC Ensembl
chr11:68402501..68484503hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3882003
hg1982003
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466240
Supporting Variants
Samples
Known GenesGAL, MTL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187875
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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