A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267821



Internal ID20477039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26596368..26596450hg38UCSC Ensembl
chr1:26922859..26922941hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739736
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267821
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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