A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3204654



Internal ID22353469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113726182..113726245hg38UCSC Ensembl
chr13:114429155..114429218hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2503n152
Supporting Variantsnssv14459005
SamplesHG00733
Known GenesGRK1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3204654
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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