A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006139



Internal ID20573179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98575948..98589245hg38UCSC Ensembl
chr12:98969726..98983023hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3813298
hg1913298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465042
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006139
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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