A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472941



Internal ID21130494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:18824773..18847859hg38UCSC Ensembl
chr12:18977707..19000793hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3823087
hg1923087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17999611
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472941
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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