A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372310



Internal ID21029863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179484684..179488663hg38UCSC Ensembl
chr3:179202472..179206451hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg383980
hg193980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099777
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372310
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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