A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150143



Internal ID21468543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104021254..104021254hg38UCSC Ensembl
chr9:106783535..106783535hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5643040
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150143
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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