A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470418



Internal ID21127971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12318191..12328029hg38UCSC Ensembl
chr12:12471125..12480963hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg389839
hg199839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998776
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470418
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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