A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673156



Internal ID9939261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:63715307..63728875hg38UCSC Ensembl
Outerchr8:63715270..63728925hg38UCSC Ensembl
Innerchr8:64627865..64641433hg19UCSC Ensembl
Outerchr8:64627828..64641483hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3813656
hg1913656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6433892
SamplesNA18634
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673156
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