A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456392



Internal ID21113945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98509085..98514906hg38UCSC Ensembl
chr12:98902863..98908684hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg385822
hg195822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006118
Samples
Known GenesTMPO-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456392
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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