A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14450488



Internal ID22245657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72658549..72658808hg38UCSC Ensembl
chr3:72707700..72707959hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3183697
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)nssv14450488
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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