A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370832



Internal ID21028385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106635625..106638431hg38UCSC Ensembl
chr3:106354472..106357278hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg382807
hg192807
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207190
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370832
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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