A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613236



Internal ID20986307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109381301..109383400hg38UCSC Ensembl
chr6:109702504..109704603hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216795
Samples
Known GenesCD164
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613236
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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