A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437884



Internal ID21095437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14358101..14361400hg38UCSC Ensembl
chr11:14379647..14382946hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183260
Samples
Known GenesRRAS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437884
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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