A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579437



Internal ID21771480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104862738..104862738hg38UCSC Ensembl
chr9:107625019..107625019hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092270
Supporting Variants
Samples
Known GenesABCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579437
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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