A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206986



Internal ID22355454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:775144..781885hg38UCSC Ensembl
chr10:821084..827825hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg386742
hg196742
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14453444, nssv14452931
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206986
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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