A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659179



Internal ID9925284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170255450..170258783hg38UCSC Ensembl
chr6:170564538..170567871hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg383334
hg193334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6071270
SamplesHG01366
Known GenesLOC154449
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659179
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer