A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3171077



Internal ID22331094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:82259991..82270229hg38UCSC Ensembl
chr6:82969708..82979946hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3810239
hg1910239
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7994n152
Supporting Variantsnssv14426043
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)nsv3171077
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