A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360156



Internal ID21017709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:82918135..83013974hg38UCSC Ensembl
chr3:82967286..83063125hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3895840
hg1995840
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210071
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360156
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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