A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3175171



Internal ID22333212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184752012..184755788hg38UCSC Ensembl
chr3:184469800..184473576hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg383777
hg193777
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6289n152
Supporting Variantsnssv14408991, nssv14408990
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3175171
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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