A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605441



Internal ID20978512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116668875..116669427hg38UCSC Ensembl
chr6:116990038..116990590hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214532
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605441
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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