A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060152



Internal ID21415201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11882728..11882728hg38UCSC Ensembl
chr1:11942785..11942785hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608662
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060152
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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