A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095975



Internal ID22005208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72647782..72647782hg38UCSC Ensembl
chr9:75262698..75262698hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382118
hg192118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588160
Samples
Known GenesTMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095975
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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