A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328457



Internal ID20861605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101803040..101803634hg38UCSC Ensembl
chr1:102268596..102269190hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050034
Samples
Known GenesOLFM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328457
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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