A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006111



Internal ID20573151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:983553..985776hg38UCSC Ensembl
chr12:1092719..1094942hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg382224
hg192224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465071
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006111
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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