A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208962



Internal ID22357111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16586156..16586258hg38UCSC Ensembl
chr17:16489470..16489572hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14406704
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)nsv3208962
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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