A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399049



Internal ID21056602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:111567001..111576900hg38UCSC Ensembl
chr5:110902699..110912597hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg389900
hg199899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213350
Samples
Known GenesSTARD4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399049
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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