A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296435



Internal ID20505653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226944702..226944766hg38UCSC Ensembl
chr1:227132403..227132467hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749144
Supporting Variants
Samples
Known GenesADCK3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296435
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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