A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579560



Internal ID21771603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38688878..38688878hg38UCSC Ensembl
chr9:38688875..38688875hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6084590
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579560
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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