A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3187640



Internal ID22339836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23277285..23284743hg38UCSC Ensembl
chr1:23603778..23611236hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg387459
hg197459
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv140n152
Supporting Variantsnssv14413807
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)nsv3187640
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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