A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373349



Internal ID21030902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22862144..23015768hg38UCSC Ensembl
chr4:22863767..23017391hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38153625
hg19153625
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212867
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373349
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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