A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368355



Internal ID21025908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37045701..37052646hg38UCSC Ensembl
chr3:37087192..37094137hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg386946
hg196946
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211183
Samples
Known GenesLRRFIP2, MLH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368355
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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