A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155166



Internal ID22085671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:39296025..39299987hg38UCSC Ensembl
Outerchr15:39295103..39305425hg38UCSC Ensembl
Innerchr15:39588226..39592188hg19UCSC Ensembl
Outerchr15:39587304..39597626hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3810323
hg1910323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011055, nssv4011046, nssv4011047, nssv4011052, nssv4011049, nssv4011054, nssv4011051, nssv4011057, nssv4011056, nssv4011053, nssv4011050, nssv4011048
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155166
Frequency
Sample Size131
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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