A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597536



Internal ID21789579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16855576..16855576hg38UCSC Ensembl
chr11:16877123..16877123hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092204
Supporting Variants
Samples
Known GenesPLEKHA7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597536
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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