A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404227



Internal ID21061780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79583656..79657825hg38UCSC Ensembl
chr5:78879479..78953648hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3874170
hg1974170
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214188
Samples
Known GenesPAPD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404227
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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