A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3954982



Internal ID21375052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75091476..75091476hg38UCSC Ensembl
chr1:75557160..75557160hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194934
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3954982
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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