A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412010



Internal ID21069563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:86107111..86153469hg38UCSC Ensembl
chr5:85402929..85449287hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3846359
hg1946359
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214303
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412010
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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