A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616658



Internal ID20989729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112545101..112553700hg38UCSC Ensembl
chr6:112866303..112874902hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg388600
hg198600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216830
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616658
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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