A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3940996



Internal ID21361065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59233701..59233701hg38UCSC Ensembl
chr18:56900933..56900933hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15185905
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3940996
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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