A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3181981



Internal ID22336853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:103810494..103810581hg38UCSC Ensembl
chr2:104426952..104427039hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14420242
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3181981
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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