A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415412



Internal ID21072965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142082733..142085338hg38UCSC Ensembl
chr5:141462298..141464903hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg382606
hg192606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125824
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415412
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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