A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14450655



Internal ID22220638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:5967137..5967945hg38UCSC Ensembl
chr4:5968864..5969672hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38809
hg19809
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3187027
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)nssv14450655
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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