A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3178493



Internal ID22335016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17172042..17173728hg38UCSC Ensembl
chr5:17172151..17173837hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg381687
hg191687
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14398618
SamplesNA19240
Known GenesLOC285696
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3178493
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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