A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17531167



Internal ID21855523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:187072734..187073094hg38UCSC Ensembl
chr1:187041866..187042226hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982224
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17531167
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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