A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462640



Internal ID21120193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:41082008..41093457hg38UCSC Ensembl
chr12:41475810..41487259hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3811450
hg1911450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1528n223
Supporting Variantsnssv18000842
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462640
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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