A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066122



Internal ID21444506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:789481..789481hg38UCSC Ensembl
chr1:724861..724861hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg382344
hg192344
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604957
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066122
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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