A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14448254



Internal ID22223054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37545789..37545966hg38UCSC Ensembl
chr19:38036691..38036868hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3208783
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14448254
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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