A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448993



Internal ID21106546
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 StatusM
Merged Variants
Supporting Variantsnssv18195198
Samples
Known GenesRRAS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448993
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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