A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408571



Internal ID21066124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:111806281..111829210hg38UCSC Ensembl
chr5:111141978..111164907hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3822930
hg1922930
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212421
Samples
Known GenesNREP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408571
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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