A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3933882



Internal ID21353951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152880979..152880979hg38UCSC Ensembl
chr1:152853455..152853455hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15186955
SamplesHG002
Known GenesSMCP
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3933882
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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