A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397730



Internal ID21055283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67817965..67889726hg38UCSC Ensembl
chr5:67113793..67185554hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg3871762
hg1971762
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214860
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397730
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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