A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17533659



Internal ID21858015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9832159..9833322hg38UCSC Ensembl
chr1:9892217..9893380hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381164
hg191164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5985472
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17533659
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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