A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667180



Internal ID9933285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62597315..62607021hg38UCSC Ensembl
Outerchr9:62596944..62607391hg38UCSC Ensembl
Innerchr9:46908616..46918322hg19UCSC Ensembl
Outerchr9:46908245..46918692hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3810448
hg1910448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5702229, essv6551762, essv5824585, essv6279138, essv5510529, essv5744409, essv5447321, essv5865098, essv5863313, essv6520977, essv5699495, essv6032731, essv5881299, essv6458658, essv6493783, essv6551019, essv6430032, essv5571437, essv6534445, essv6166398, essv5577091, essv6277731, essv6573095, essv5526028, essv5574102, essv6529257, essv5910055
SamplesNA19664, NA19746, NA19728, NA19723, NA19681, NA19720, NA19722, NA19657, NA19717, NA19663, NA19776, NA19682, NA19675, NA19729, NA19652, NA19747, NA19773, NA19679, NA19786, NA19783, NA19759, NA19779, NA19716, NA19770, NA19726, NA19661, NA19758
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667180
Frequency
Sample Size1151
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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