A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409080



Internal ID21066633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:81217794..81228650hg38UCSC Ensembl
chr6:81927511..81938367hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3810857
hg1910857
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229294
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409080
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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