A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066446



Internal ID21445029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7803433..7803433hg38UCSC Ensembl
chr1:7863493..7863493hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618319
Supporting Variants
SamplesHG00732
Known GenesPER3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066446
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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