A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280846



Internal ID20490064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241108969..241109049hg38UCSC Ensembl
chr2:242048384..242048464hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745419
Supporting Variants
Samples
Known GenesPASK
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280846
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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