A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375187



Internal ID21032740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:79125898..79125973hg38UCSC Ensembl
chr3:79175048..79175123hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104547
Samples
Known GenesROBO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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