A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3178182



Internal ID22334844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152306501..152307472hg38UCSC Ensembl
chr1:152278977..152279948hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38972
hg19972
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv422n152
Supporting Variantsnssv14413256
SamplesHG00514
Known GenesFLG
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3178182
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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