A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094064



Internal ID20661104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:12659315..12661441hg38UCSC Ensembl
chr3:12700814..12702940hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg382127
hg192127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369101
Supporting Variants
Samples
Known GenesRAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094064
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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