A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457576



Internal ID21115129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:89406908..89412393hg38UCSC Ensembl
chr12:89800685..89806170hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg385486
hg195486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004848
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457576
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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