A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369697



Internal ID21027250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65091653..65099531hg38UCSC Ensembl
chr3:65077328..65085206hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg387879
hg197879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101552
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369697
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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