A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095156



Internal ID22004389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43109344..43109344hg38UCSC Ensembl
chr9:42875890..42875890hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586103
Samples
Known GenesAQP7P3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095156
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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