A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290532



Internal ID20499750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209449884..209449948hg38UCSC Ensembl
chr1:209623229..209623293hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748021
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290532
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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