A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1498e214



Internal ID22757392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104604904..104618230hg38UCSC Ensembl
chr9:107367185..107380511hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3813327
hg1913327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3621336, esv3621338
SamplesNA19394, NA19378, HG02860, NA19038, HG02703, NA19383, NA19901, HG02009, NA19462, NA19043, NA19449, HG03446, NA19320, NA19017, NA19308, NA19434, NA19019, NA19473, NA19380, NA19324, NA19360, NA19143
Known GenesOR13C2, OR13C9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1498e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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