A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611428



Internal ID6651647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160167929..160379860hg38UCSC Ensembl
chr6:160588961..160800892hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38211932
hg19211932
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12612058
SamplesNA18953
Known GenesSLC22A2, SLC22A3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611428
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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