A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089375



Internal ID21998608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16888302..16888302hg38UCSC Ensembl
chr11:16909849..16909849hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593729
Samples
Known GenesPLEKHA7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089375
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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