A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364047



Internal ID21021600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142868501..143010800hg38UCSC Ensembl
chr3:142587343..142729642hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38142300
hg19142300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209668
Samples
Known GenesLOC100289361, LOC100507389, PAQR9, PCOLCE2, U2SURP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364047
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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