A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3171749



Internal ID22331455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172787219..172787298hg38UCSC Ensembl
chr5:172214222..172214301hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14399198
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3171749
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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