A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389149



Internal ID21046702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:27456622..27502869hg38UCSC Ensembl
chr5:27456729..27502976hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3846248
hg1946248
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215757
Samples
Known GenesLINC01021
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389149
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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