A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094356



Internal ID22003589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87845046..87845046hg38UCSC Ensembl
chr9:90459961..90459961hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg382637
hg192637
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592719
Samples
Known GenesCTSLP8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094356
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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