A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14460821



Internal ID22213386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43541207..43542098hg38UCSC Ensembl
chr5:43541309..43542200hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38892
hg19892
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3185007
Supporting Variants
SamplesHG00733
Known GenesPAIP1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14460821
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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