A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363417



Internal ID21020970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78832965..78833423hg38UCSC Ensembl
chr3:78882115..78882573hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103893
Samples
Known GenesROBO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363417
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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