A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187589



Internal ID20754629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133456210..133506769hg38UCSC Ensembl
chr11:133326105..133376664hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3850560
hg1950560
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461769
Supporting Variants
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187589
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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