A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387111



Internal ID21044664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170702342..170712882hg38UCSC Ensembl
chr4:171623493..171634033hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3810541
hg1910541
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213883
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387111
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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