A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421112



Internal ID21078665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3142001..3146600hg38UCSC Ensembl
chr9:3142001..3146600hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg384600
hg194600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224801
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421112
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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