A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3544901



Internal ID22413922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13918346..13919778hg38UCSC Ensembl
chr18:13918345..13919777hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg381433
hg191433
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14458974
SamplesHG00732
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3544901
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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