A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603646



Internal ID20976717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127593957..127637456hg38UCSC Ensembl
chr6:127915102..127958601hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg3843500
hg1943500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603646
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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