A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060620



Internal ID21414133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149904818..149904818hg38UCSC Ensembl
chr1:149876370..149876370hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3818045
hg1918045
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613521
Supporting Variants
SamplesHG00513
Known GenesSV2A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060620
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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