A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414886



Internal ID21072439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9969301..9970900hg38UCSC Ensembl
chr6:9969534..9971133hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414886
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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