A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276428



Internal ID20485646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207142884..207143206hg38UCSC Ensembl
chr1:207316229..207316551hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738189
Supporting Variants
Samples
Known GenesC4BPA
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276428
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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