A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435964



Internal ID22493834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27219685..27219685hg38UCSC Ensembl
chr9:27219683..27219683hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5957078
Supporting Variants
Samples
Known GenesTEK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435964
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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