A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210273



Internal ID22358217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:2231789..2231845hg38UCSC Ensembl
chr10:2273983..2274039hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14390992
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)nsv3210273
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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