A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198615



Internal ID22348316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1626782..1630073hg38UCSC Ensembl
chr19:1626781..1630072hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383292
hg193292
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4061n152
Supporting Variantsnssv14455757, nssv14460123
SamplesHG00733
Known GenesTCF3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198615
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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