A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613389



Internal ID20986460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134632901..134635900hg38UCSC Ensembl
chr6:134954039..134957038hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215608
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613389
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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