A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467439



Internal ID21124992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94642201..94647400hg38UCSC Ensembl
chr11:94375367..94380566hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1277n223
Supporting Variantsnssv18187000
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467439
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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