A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621338



Internal ID7008207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104605107..104618230hg38UCSC Ensembl
Innerchr9:104605607..104617730hg38UCSC Ensembl
Outerchr9:104604107..104619230hg38UCSC Ensembl
chr9:107367388..107380511hg19UCSC Ensembl
Innerchr9:107367888..107380011hg19UCSC Ensembl
Outerchr9:107366388..107381511hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3813124
hg1913124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1498e214
Supporting Variantsessv13591870, essv13591872, essv13591884, essv13591878, essv13591888, essv13591879, essv13591887, essv13591876, essv13591886, essv13591877, essv13591875, essv13591891, essv13591890, essv13591881, essv13591880, essv13591882, essv13591873, essv13591889, essv13591871, essv13591885, essv13591883, essv13591874
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)esv3621338
Frequency
Sample Size2504
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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