A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3184657



Internal ID22338269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71927216..71927388hg38UCSC Ensembl
chr3:71976367..71976539hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14423037
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3184657
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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