A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411982



Internal ID21069535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:51514350..51548710hg38UCSC Ensembl
chr6:51379148..51413508hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3834361
hg1934361
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218342
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411982
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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