A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354845



Internal ID21012398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:47821260..47821874hg38UCSC Ensembl
chr2:48048399..48049013hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089419
Samples
Known GenesFBXO11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354845
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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