A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450128



Internal ID21107681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131904165..131904471hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978510
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450128
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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