A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17529654



Internal ID21854011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:188017942..188023258hg38UCSC Ensembl
chr1:187987073..187992389hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg385317
hg195317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982226
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17529654
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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