A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3532631



Internal ID22401958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11100556..11100556hg38UCSC Ensembl
chr2:11240682..11240682hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381847
hg191847
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14448284
SamplesHG00733
Known GenesFLJ33534
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3532631
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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