A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415029



Internal ID21072582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:66511201..66532800hg38UCSC Ensembl
chr6:67221094..67242693hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3821600
hg1921600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6235n223
Supporting Variantsnssv18235919
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415029
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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