A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363912



Internal ID21021465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187998725..188001663hg38UCSC Ensembl
chr3:187716513..187719451hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg382939
hg192939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100232
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363912
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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