A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14453486



Internal ID22217762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100371908..100371976hg38UCSC Ensembl
chr4:101293065..101293133hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3175376
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)nssv14453486
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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