A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1478e214



Internal ID22757372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61660998..61699030hg38UCSC Ensembl
chr9:44868836..44906868hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3838033
hg1938033
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3620500, esv3620501
SamplesHG02661, HG00743, HG03571, HG02654, NA19758
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1478e214
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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