A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170835



Internal ID22330958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:134441112..134442902hg38UCSC Ensembl
chr5:133776803..133778593hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg381791
hg191791
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7530n152
Supporting Variantsnssv14424687
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3170835
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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