A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18002913



Internal ID20569953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:71795379..71796793hg38UCSC Ensembl
chr12:72189159..72190573hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg381415
hg191415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472749
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18002913
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.23025


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