A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364111



Internal ID21021664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78993146..78993716hg38UCSC Ensembl
chr3:79042296..79042866hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104525
Samples
Known GenesROBO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364111
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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