A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936550



Internal ID21356619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11959476..11959552hg38UCSC Ensembl
chr18:11959475..11959551hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15175779
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936550
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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