A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674410



Internal ID9940515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:13671083..13671687hg38UCSC Ensembl
Outerchr6:13671046..13671737hg38UCSC Ensembl
Innerchr6:13671315..13671919hg19UCSC Ensembl
Outerchr6:13671278..13671969hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38692
hg19692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5995504
SamplesHG00442
Known GenesRANBP9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674410
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