A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617522



Internal ID7004407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:68315517..68391767hg38UCSC Ensembl
chr8:69227752..69304002hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3876251
hg1976251
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13218301
SamplesHG02406
Known GenesC8orf34, LOC286189
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617522
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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