A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3187297



Internal ID22339651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182376996..182377365hg38UCSC Ensembl
chr4:183298149..183298518hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14451948
SamplesHG00733
Known GenesTENM3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3187297
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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