A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361951



Internal ID21019504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86998899..87005748hg38UCSC Ensembl
chr3:87048049..87054898hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg386850
hg196850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104141
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361951
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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