A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14451027



Internal ID22220260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16309520..16309609hg38UCSC Ensembl
chr3:16351027..16351116hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3177351
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)nssv14451027
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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