A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162098



Internal ID21457258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5677583..5677583hg38UCSC Ensembl
chr9:5677583..5677583hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639605
Supporting Variants
SamplesHG02587
Known GenesKIAA1432
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162098
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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