A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609991



Internal ID20983062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163634459..163721287hg38UCSC Ensembl
chr6:164055491..164142319hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3886829
hg1986829
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216989
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609991
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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