A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399043



Internal ID21056596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79352269..79365087hg38UCSC Ensembl
chr5:78648092..78660910hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3812819
hg1912819
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133422
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399043
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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