A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459683



Internal ID21117236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3321298..3331664hg38UCSC Ensembl
chr12:3430464..3440830hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg3810367
hg1910367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000823
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459683
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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