A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199539



Internal ID22349108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1626777..1630071hg38UCSC Ensembl
chr19:1626776..1630070hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383295
hg193295
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4061n152
Supporting Variantsnssv14407319, nssv14407318
SamplesNA19240
Known GenesTCF3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199539
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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