A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620307



Internal ID7007178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32709381..32736093hg38UCSC Ensembl
chr9:32709379..32736091hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3826713
hg1926713
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1470e214
Supporting Variantsessv13451386, essv13451390, essv13451389, essv13451384, essv13451385, essv13451388, essv13451387, essv13451391
SamplesHG03485, NA18516, HG01989, HG03024, NA19321, NA19143, HG04098, NA19429
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620307
Frequency
Sample Size2504
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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