A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3188067



Internal ID22340059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31764431..31764925hg38UCSC Ensembl
chr1:32230032..32230526hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14440575
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)nsv3188067
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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