A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612787



Internal ID20985858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:129824249..129828081hg38UCSC Ensembl
chr6:130145394..130149226hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg383833
hg193833
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215543
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612787
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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