A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060619



Internal ID21414135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149891609..149891609hg38UCSC Ensembl
chr1:149863159..149863159hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3818052
hg1918052
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605236
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060619
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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