A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468804



Internal ID21126357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97596196..97812423hg38UCSC Ensembl
chr11:97467196..97683423hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38216228
hg19216228
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194665
Samples
Known GenesMIR7976
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468804
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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