A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3930869



Internal ID21350938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76975154..76975154hg38UCSC Ensembl
chr18:74687110..74687110hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15184545
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3930869
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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