A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600749



Internal ID21792796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:80786294..80795121hg38UCSC Ensembl
chr12:81180073..81188900hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg388828
hg198828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024073
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600749
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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