A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378299



Internal ID21035852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2108901..2110068hg38UCSC Ensembl
chr5:2109015..2110182hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381168
hg191168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129296
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378299
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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