A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620126



Internal ID7006999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27247574..27295787hg38UCSC Ensembl
chr9:27247572..27295785hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3848214
hg1948214
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13433606
SamplesNA19309
Known GenesEQTN, LINC00032
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620126
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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