A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413786



Internal ID21071339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167357466..167371488hg38UCSC Ensembl
chr5:166784471..166798493hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3814023
hg1914023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129473
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413786
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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