A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14397921



Internal ID22294916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37901683..37901814hg38UCSC Ensembl
chr4:37903304..37903435hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3172260
Supporting Variants
SamplesNA19240
Known GenesTBC1D1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14397921
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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