A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17161451



Internal ID21443191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26104450..26104450hg38UCSC Ensembl
chr9:26104448..26104448hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5625587
Supporting Variants
SamplesHG00732
Known GenesLOC100506422
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17161451
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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