A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361438



Internal ID21018991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160225401..160227500hg38UCSC Ensembl
chr3:159943188..159945287hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207982
Samples
Known GenesC3orf80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361438
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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