A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14413683



Internal ID22149013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145295690..145305160hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg389471
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3171058
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14413683
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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