A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17448197



Internal ID22506067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77012119..77012119hg38UCSC Ensembl
chr9:79627035..79627035hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5966414
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17448197
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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