A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611603



Internal ID20984674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:130448652..130458108hg38UCSC Ensembl
chr6:130769797..130779253hg19UCSC Ensembl
Cytoband6q23.1
Allele length
AssemblyAllele length
hg389457
hg199457
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215551
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611603
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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