A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14460099



Internal ID22212644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177468013..177468069hg38UCSC Ensembl
chr5:176895014..176895070hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3179635
Supporting Variants
SamplesHG00733
Known GenesDBN1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14460099
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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