A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588783



Internal ID21780826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28430843..28430896hg38UCSC Ensembl
chr11:28452390..28452443hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036583
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588783
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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