A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262224



Internal ID20471442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179692073..179692289hg38UCSC Ensembl
chr1:179661208..179661424hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731850
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262224
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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