A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196064



Internal ID22346143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9364768..9367007hg38UCSC Ensembl
chr10:9406731..9408970hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382240
hg192240
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv787n152
Supporting Variantsnssv14441473, nssv14414904
SamplesHG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196064
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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