A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583110



Internal ID21775153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101892192..101896845hg38UCSC Ensembl
chr11:101762923..101767576hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg384654
hg194654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032051
Supporting Variants
Samples
Known GenesANGPTL5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583110
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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