A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286536



Internal ID20495754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67358585..67366463hg38UCSC Ensembl
chr1:67824268..67832146hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg387879
hg197879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747613
Supporting Variants
Samples
Known GenesIL12RB2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286536
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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