A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372973



Internal ID21030526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148695001..148699800hg38UCSC Ensembl
chr3:148412788..148417587hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211395
Samples
Known GenesAGTR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372973
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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