A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467174



Internal ID21124727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118817417..118817964hg38UCSC Ensembl
chr11:118688126..118688673hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38548
hg19548
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467174
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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