A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154654



Internal ID22085159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:112078848..112092083hg38UCSC Ensembl
Outerchr10:112077880..112094141hg38UCSC Ensembl
Innerchr10:113838606..113851841hg19UCSC Ensembl
Outerchr10:113837638..113853899hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3816262
hg1916262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004467
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154654
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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