A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006141



Internal ID20573181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98582944..98591489hg38UCSC Ensembl
chr12:98976722..98985267hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg388546
hg198546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466542
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006141
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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