A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332405



Internal ID20865576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:230710298..230737011hg38UCSC Ensembl
chr1:230846044..230872757hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3826714
hg1926714
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202768
Samples
Known GenesAGT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332405
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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