A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463040



Internal ID21120593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:83156636..83158552hg38UCSC Ensembl
chr12:83550415..83552331hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg381917
hg191917
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004596
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463040
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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