A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178379



Internal ID20745419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77652592..77688163hg38UCSC Ensembl
chr11:77363637..77399208hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3835572
hg1935572
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464627
Supporting Variants
Samples
Known GenesRSF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178379
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00023


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