A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190618



Internal ID22341457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132192012..132192066hg38UCSC Ensembl
chr10:134005516..134005570hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14440749
SamplesHG00733
Known GenesDPYSL4
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190618
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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