A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409876



Internal ID21067429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154865933..154870237hg38UCSC Ensembl
chr5:154245493..154249797hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg384305
hg194305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128757
Samples
Known GenesCNOT8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409876
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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