A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333880



Internal ID20867061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145488103..148061210hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382573108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051742
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333880
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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