A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487313



Internal ID21144866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:116326296..116327697hg38UCSC Ensembl
chr12:116764101..116765502hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997135
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487313
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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