A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14457283



Internal ID22251369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121903248..121903304hg38UCSC Ensembl
chr4:122824403..122824459hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3175121
Supporting Variants
SamplesHG00733
Known GenesTRPC3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14457283
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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