A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191403



Internal ID20758444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20065276..20153771hg38UCSC Ensembl
chr11:20086822..20175317hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3888496
hg1988496
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442305
Supporting Variants
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191403
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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