A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459368



Internal ID21116921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9844967..9894173hg38UCSC Ensembl
chr12:9997566..10046772hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3849207
hg1949207
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185275
Samples
Known GenesCLEC2B, KLRF1, KLRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459368
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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