A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062481



Internal ID21415069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:213602014..213602014hg38UCSC Ensembl
chr1:213775357..213775357hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624067
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062481
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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