A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460242



Internal ID21117795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46752541..46753109hg38UCSC Ensembl
chr12:47146324..47146892hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001727
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460242
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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