A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626920



Internal ID21818967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63048..63139hg38UCSC Ensembl
chr11:128733..128824hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038136
Supporting Variants
Samples
Known GenesLINC01001
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626920
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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