A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461304



Internal ID21118857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:39386090..39386704hg38UCSC Ensembl
chr12:39779892..39780506hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000324
Samples
Known GenesKIF21A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461304
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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