A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411604



Internal ID21069157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140612301..140615100hg38UCSC Ensembl
chr5:139991886..139994685hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5956n223
Supporting Variantsnssv18125157
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411604
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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