A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369476



Internal ID21027029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184029143..184033774hg38UCSC Ensembl
chr3:183746931..183751562hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg384632
hg194632
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212161
Samples
Known GenesHTR3D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369476
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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