A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364663



Internal ID21022216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72114873..72176776hg38UCSC Ensembl
chr3:72164024..72225927hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3861904
hg1961904
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208697
Samples
Known GenesLINC00870
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364663
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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