A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17115269



Internal ID21452825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:94579575..94579575hg38UCSC Ensembl
chr9:67020990..67020990hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38995
hg19995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622053
Supporting Variants
SamplesHG02011
Known GenesLOC286297
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17115269
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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