A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3186264



Internal ID22339106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202203775..202206437hg38UCSC Ensembl
chr1:202172903..202175565hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382663
hg192663
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv528n152
Supporting Variantsnssv14433907, nssv14433908
SamplesHG00514
Known GenesLGR6
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3186264
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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