A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3171602



Internal ID22331385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13925069..13925262hg38UCSC Ensembl
chr6:13925300..13925493hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7750n152
Supporting Variantsnssv14425922
SamplesHG00514
Known GenesRNF182
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3171602
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