A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281202



Internal ID20490420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203525034..203525266hg38UCSC Ensembl
chr1:203494162..203494394hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739687
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281202
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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