A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332322



Internal ID20865492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171275858..171276594hg38UCSC Ensembl
chr1:171244997..171245733hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg38737
hg19737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053848
Samples
Known GenesFMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332322
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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