A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621132



Internal ID6661312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94553429..94583540hg38UCSC Ensembl
chr9:97315711..97345822hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3830112
hg1930112
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1493e214
Supporting Variantsessv13570791
SamplesHG04229
Known GenesFBP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621132
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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