A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610831



Internal ID6997748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132173440..132194785hg38UCSC Ensembl
chr6:132494580..132515925hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3821346
hg1921346
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12553382, essv12553383, essv12553381, essv12553380, essv12553384, essv12553385, essv12553378, essv12553377, essv12553379
SamplesHG03947, NA21129, HG03862, HG02697, HG02728, HG03823, HG03021, HG03019, HG04198
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610831
Frequency
Sample Size2504
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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