A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459389



Internal ID21116942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:28674801..28680600hg38UCSC Ensembl
chr12:28827734..28833533hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998507
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459389
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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