A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460007



Internal ID21117560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64676202..64684460hg38UCSC Ensembl
chr12:65069982..65078240hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg388259
hg198259
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180993
Samples
Known GenesRASSF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460007
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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