A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369505



Internal ID21027058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16814981..16827679hg38UCSC Ensembl
chr3:16856483..16869178hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3812699
hg1912696
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208596
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369505
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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