A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610922



Internal ID6997838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136532552..136546029hg38UCSC Ensembl
chr6:136853690..136867167hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3813478
hg1913478
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12561521
SamplesNA19472
Known GenesMAP7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610922
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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