A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363092



Internal ID21020645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62890836..62900998hg38UCSC Ensembl
chr3:62876511..62886673hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3810163
hg1910163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101807
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363092
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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