A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410063



Internal ID21067616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61304741..61306917hg38UCSC Ensembl
chr5:60600568..60602744hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg382177
hg192177
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216254
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410063
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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