A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14436859



Internal ID22180032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149648568..149652541hg38UCSC Ensembl
chr5:149028131..149032104hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg383974
hg193974
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3182978
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)nssv14436859
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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