A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154673



Internal ID22085178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4228783..4338058hg38UCSC Ensembl
Outerchr11:4217824..4363567hg38UCSC Ensembl
Innerchr11:4250013..4359288hg19UCSC Ensembl
Outerchr11:4239054..4384797hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38145744
hg19145744
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv42n97
Supporting Variantsnssv4005564, nssv4005559, nssv4005562, nssv4005560, nssv4005563, nssv4005561, nssv4005566, nssv4005565
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154673
Frequency
Sample Size131
Observed Gain3
Observed Loss5
Observed Complex0
Frequencyn/a


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