A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292402



Internal ID20501620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:94177141..94177221hg38UCSC Ensembl
chr12:94570917..94570997hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731115
Supporting Variants
Samples
Known GenesPLXNC1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292402
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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