A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361461



Internal ID21019014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87000140..87017679hg38UCSC Ensembl
chr3:87049290..87066829hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3817540
hg1917540
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210163
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361461
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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