A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192892



Internal ID22343415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70263434..70263564hg38UCSC Ensembl
chr10:72023190..72023320hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14442425
SamplesHG00733
Known GenesNPFFR1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192892
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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