A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361877



Internal ID21019430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:66789264..66790048hg38UCSC Ensembl
chr3:66839688..66840472hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38785
hg19785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103586
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361877
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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