A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491250



Internal ID21148803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111029784..111030542hg38UCSC Ensembl
chr12:111467588..111468346hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38759
hg19759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996954
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491250
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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