A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201319



Internal ID22350649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34838354..34838493hg38UCSC Ensembl
chr17:33165373..33165512hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14431981
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)nsv3201319
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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