A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413220



Internal ID21070773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:100784960..100897256hg38UCSC Ensembl
chr5:100120664..100232960hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38112297
hg19112297
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214451
Samples
Known GenesST8SIA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413220
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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