A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3184865



Internal ID22338385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158846021..158846227hg38UCSC Ensembl
chr4:159767173..159767379hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14452503
SamplesHG00733
Known GenesFNIP2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3184865
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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