A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360387



Internal ID21017940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189036808..189037219hg38UCSC Ensembl
chr3:188754597..188755008hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100285
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360387
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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