A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357317



Internal ID21014870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72686694..72691502hg38UCSC Ensembl
chr3:72735845..72740653hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg384809
hg194809
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208700
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357317
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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