A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3194801



Internal ID22345070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7870900..7870969hg38UCSC Ensembl
chr19:7935786..7935855hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14432386, nssv14457543
SamplesHG00733, HG00514
Known GenesFLJ22184
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3194801
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer