A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358763



Internal ID21016316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4009545..4097269hg38UCSC Ensembl
chr3:4051229..4138953hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3887725
hg1987725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4766n223
Supporting Variantsnssv18100925
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358763
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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