A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580878



Internal ID21772921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102828862..102828926hg38UCSC Ensembl
chr11:102699593..102699657hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027397
Supporting Variants
Samples
Known GenesWTAPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580878
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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