A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356069



Internal ID21013622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:79776178..79777631hg38UCSC Ensembl
chr3:79825328..79826781hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg381454
hg191454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102582
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356069
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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