A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3172339



Internal ID22331757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9243590..9243763hg38UCSC Ensembl
chr3:9285274..9285447hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14460146
SamplesHG00733
Known GenesSRGAP3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3172339
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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