A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467827



Internal ID21125380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95033401..95039500hg38UCSC Ensembl
chr11:94766565..94772664hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg386100
hg196100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467827
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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