A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17591809



Internal ID21783852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62277957..62278016hg38UCSC Ensembl
chr11:62045429..62045488hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028689
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17591809
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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