A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494788



Internal ID21152341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:115888897..115903834hg38UCSC Ensembl
chr12:116326702..116341639hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg3814938
hg1914938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997113
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494788
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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