A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550695



Internal ID15991418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42956988..43121303hg38UCSC Ensembl
Innerchr10:43452436..43616751hg19UCSC Ensembl
Innerchr10:42772442..42936757hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38164316
hg19164316
hg18164316
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv747325
Samples
Known GenesMIR5100, RET
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550695
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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