A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611433



Internal ID6651652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160246104..160312952hg38UCSC Ensembl
chr6:160667136..160733984hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3866849
hg1966849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1231e214
Supporting Variantsessv12612133
SamplesNA20813
Known GenesSLC22A2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611433
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