A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407755



Internal ID21065308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79215124..79222525hg38UCSC Ensembl
chr5:78510947..78518348hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg387402
hg197402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214181
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407755
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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