A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473608



Internal ID21131161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127927425..127956352hg38UCSC Ensembl
chr11:127797320..127826247hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3828928
hg1928928
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184367
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473608
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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