A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460390



Internal ID21117943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:105628020..105679198hg38UCSC Ensembl
chr12:106021798..106072976hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3851179
hg1951179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995980
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460390
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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