A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467934



Internal ID21125487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121290601..121296300hg38UCSC Ensembl
chr11:121161310..121167009hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186588
Samples
Known GenesSC5D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467934
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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