A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17586717



Internal ID21778760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75068436..75068436hg38UCSC Ensembl
chr9:77683352..77683352hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg383416
hg193416
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6081171
Supporting Variants
Samples
Known GenesNMRK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17586717
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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