A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190950



Internal ID22341733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13052733..13053109hg38UCSC Ensembl
chr19:13163547..13163923hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14462140
SamplesHG00733
Known GenesNFIX
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190950
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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