A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3948676



Internal ID21368745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9058020..9058020hg38UCSC Ensembl
chr18:9058018..9058018hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15184470, nssv15184471
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3948676
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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