A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154612



Internal ID22085117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65445150..65480454hg38UCSC Ensembl
Outerchr10:65443747..65483619hg38UCSC Ensembl
Innerchr10:67204908..67240212hg19UCSC Ensembl
Outerchr10:67203505..67243377hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3839873
hg1939873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005797
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154612
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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