A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620672



Internal ID7007542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73452023..73465464hg38UCSC Ensembl
Innerchr9:73452023..73465464hg38UCSC Ensembl
Outerchr9:73451876..73465625hg38UCSC Ensembl
chr9:76066939..76080380hg19UCSC Ensembl
Innerchr9:76066939..76080380hg19UCSC Ensembl
Outerchr9:76066792..76080541hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3813442
hg1913442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13518827, essv13518828, essv13518818, essv13518823, essv13518825, essv13518826, essv13518822, essv13518829, essv13518816, essv13518819, essv13518820, essv13518830, essv13518821, essv13518831, essv13518824, essv13518817
SamplesHG03484, NA19399, HG03455, NA18878, NA18870, NA18510, NA19374, NA19024, HG03136, NA19401, NA19375, HG01915, HG03419, HG03108, NA19116, NA19121
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620672
Frequency
Sample Size2504
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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