A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399056



Internal ID21056609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27660901..27692500hg38UCSC Ensembl
chr6:27628680..27660279hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3831600
hg1931600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221331
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399056
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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