A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439782



Internal ID21097335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2166356..2179343hg38UCSC Ensembl
chr11:2187586..2200573hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3812988
hg1912988
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184099
Samples
Known GenesMIR4686, TH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439782
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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