A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360327



Internal ID21017880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4204901..4228600hg38UCSC Ensembl
chr3:4246585..4270284hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3823700
hg1923700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099882
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360327
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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