A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14432924



Internal ID22175818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72510750..72518073hg38UCSC Ensembl
chr3:72559901..72567224hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg387324
hg197324
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3173173
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)nssv14432924
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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