A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357302



Internal ID21014855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31357826..31396341hg38UCSC Ensembl
chr3:31399318..31437833hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg3838516
hg1938516
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210506
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357302
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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