A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202672



Internal ID22351800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55586539..55586601hg38UCSC Ensembl
chr16:55620451..55620513hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14380475, nssv14418937
SamplesNA19240, HG00514
Known GenesLPCAT2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202672
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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