A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192149



Internal ID22342772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68827628..68827964hg38UCSC Ensembl
chr10:70587385..70587721hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14383182, nssv14439815, nssv14437301
SamplesNA19240, HG00733, HG00514
Known GenesSTOX1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192149
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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