A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154671



Internal ID22085176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4228783..4315299hg38UCSC Ensembl
Outerchr11:4217824..4325579hg38UCSC Ensembl
Innerchr11:4250013..4336529hg19UCSC Ensembl
Outerchr11:4239054..4346809hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38107756
hg19107756
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv42n97
Supporting Variantsnssv4005544, nssv4005538, nssv4005550, nssv4005555, nssv4005546, nssv4005530, nssv4005551, nssv4005542, nssv4005527, nssv4005545, nssv4005554, nssv4005537, nssv4005534, nssv4005529, nssv4005553, nssv4005540, nssv4005526, nssv4005528, nssv4005532, nssv4005535, nssv4005541, nssv4005549, nssv4005536, nssv4005543, nssv4005547, nssv4005552, nssv4005556, nssv4005531, nssv4005533, nssv4005539, nssv4005548
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154671
Frequency
Sample Size131
Observed Gain10
Observed Loss21
Observed Complex0
Frequencyn/a


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