A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412859



Internal ID21070412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:163063391..163123978hg38UCSC Ensembl
chr5:162490397..162550984hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3860588
hg1960588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215958
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412859
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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