A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661137



Internal ID9580556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142256328..142935413hg38UCSC Ensembl
Outerchr8:142256294..142935448hg38UCSC Ensembl
Innerchr8:143337689..144016829hg19UCSC Ensembl
Outerchr8:143337655..144016864hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38679155
hg19679210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5973601
SamplesNA18907
Known GenesARC, BAI1, CYP11B1, CYP11B2, GML, JRK, LOC100288181, LY6D, LY6K, LYNX1, LYPD2, PSCA, SLURP1, THEM6, TSNARE1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661137
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