A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325942



Internal ID20859076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162009895..162050605hg38UCSC Ensembl
chr1:161979685..162020395hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3840711
hg1940711
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201888
Samples
Known GenesOLFML2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325942
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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