A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412089



Internal ID21069642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155311101..155317210hg38UCSC Ensembl
chr5:154690661..154696770hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg386110
hg196110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128783
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412089
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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