A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470489



Internal ID21128042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:65575501..65584900hg38UCSC Ensembl
chr12:65969281..65978680hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg389400
hg199400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18003007
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470489
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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