A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365877



Internal ID21023430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30421360..30440421hg38UCSC Ensembl
chr3:30462852..30481913hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3819062
hg1919062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099273
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365877
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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