A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382480



Internal ID21040033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:101134711..101527569hg38UCSC Ensembl
chr4:102055868..102448726hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38392859
hg19392859
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209433
Samples
Known GenesFLJ20021, MIR8066, PPP3CA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382480
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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