A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195198



Internal ID20762238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14363875..14366381hg38UCSC Ensembl
chr11:14385421..14387927hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg382507
hg192507
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448993
Supporting Variants
Samples
Known GenesRRAS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195198
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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