A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361289



Internal ID21018842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141462173..141473887hg38UCSC Ensembl
chr3:141181015..141192729hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3811715
hg1911715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094305
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361289
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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