A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093947



Internal ID22003180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68793110..68793110hg38UCSC Ensembl
chr9:71408026..71408026hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579780
Samples
Known GenesPIP5K1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093947
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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