A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406909



Internal ID21064462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:48815494..48830570hg38UCSC Ensembl
chr6:48783131..48798207hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3815077
hg1915077
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223462
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406909
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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