A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601418



Internal ID21793465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130091257..130092213hg38UCSC Ensembl
chr11:129961152..129962108hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38957
hg19957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036148
Supporting Variants
Samples
Known GenesAPLP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601418
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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