A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170888



Internal ID22330988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169495172..169495257hg38UCSC Ensembl
chr1:169464410..169464495hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14377005
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3170888
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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