A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154596



Internal ID22085101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48314015..48347624hg38UCSC Ensembl
Outerchr10:48310320..48351511hg38UCSC Ensembl
Innerchr10:49522058..49555667hg19UCSC Ensembl
Outerchr10:49518363..49559554hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3841192
hg1941192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004754
Samples
Known GenesMAPK8
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154596
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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