A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360747



Internal ID21018300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132643901..132646000hg38UCSC Ensembl
chr3:132362745..132364844hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094186
Samples
Known GenesACAD11, NPHP3-ACAD11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360747
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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