A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3175121



Internal ID22333186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121903248..121903304hg38UCSC Ensembl
chr4:122824403..122824459hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14457283
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)nsv3175121
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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