A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407811



Internal ID21065364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:64688917..64689376hg38UCSC Ensembl
chr5:63984744..63985203hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38460
hg19460
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214092
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407811
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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