A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154575



Internal ID22085080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43079488..43125103hg38UCSC Ensembl
Outerchr10:43075137..43127358hg38UCSC Ensembl
Innerchr10:43574936..43620551hg19UCSC Ensembl
Outerchr10:43570585..43622806hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3852222
hg1952222
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004710
Samples
Known GenesRET
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154575
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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