A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359366



Internal ID21016919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16370066..16405184hg38UCSC Ensembl
chr4:16371689..16406807hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3835119
hg1935119
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213762
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359366
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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