A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621508



Internal ID7008377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112208464..112210460hg38UCSC Ensembl
Innerchr9:112208464..112210460hg38UCSC Ensembl
Outerchr9:112208117..112210867hg38UCSC Ensembl
chr9:114970744..114972740hg19UCSC Ensembl
Innerchr9:114970744..114972740hg19UCSC Ensembl
Outerchr9:114970397..114973147hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381997
hg191997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13606104, essv13606146, essv13606116, essv13606094, essv13606132, essv13606087, essv13606090, essv13606095, essv13606133, essv13606089, essv13606130, essv13606114, essv13606084, essv13606108, essv13606134, essv13606123, essv13606137, essv13606106, essv13606124, essv13606138, essv13606097, essv13606144, essv13606093, essv13606120, essv13606121, essv13606086, essv13606096, essv13606100, essv13606139, essv13606110, essv13606141, essv13606125, essv13606098, essv13606103, essv13606142, essv13606129, essv13606107, essv13606099, essv13606147, essv13606085, essv13606113, essv13606088, essv13606119, essv13606143, essv13606118, essv13606145, essv13606092, essv13606131, essv13606115, essv13606128, essv13606102, essv13606136, essv13606127, essv13606117, essv13606112, essv13606101, essv13606122, essv13606111, essv13606126, essv13606109, essv13606140, essv13606135, essv13606105, essv13606091
SamplesHG01985, HG02890, NA19222, HG02944, HG03378, NA19914, HG02433, HG02337, HG02012, HG02589, NA18510, HG03074, NA18519, HG02621, NA19201, HG02325, NA19198, HG02595, HG02756, NA18498, HG03040, HG02922, HG02562, HG02143, HG02315, NA19385, HG02471, HG03380, HG03225, NA19209, HG02882, HG03169, HG02943, NA18934, HG02144, NA18910, HG02508, HG02497, HG02470, HG03294, NA18499, NA18853, HG02256, NA19095, NA19395, HG01956, HG02813, NA19017, NA19440, NA19309, HG01894, HG03117, NA19144, NA19835, NA19428, HG02580, HG03557, NA19472, NA18994, NA19093, NA19096, NA19030, NA19129, HG03439
Known GenesMIR3134
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621508
Frequency
Sample Size2504
Observed Gain0
Observed Loss64
Observed Complex0
Frequencyn/a


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