A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550608



Internal ID16338017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:41705581..41851479hg38UCSC Ensembl
Innerchr10:42388730..42534628hg19UCSC Ensembl
Innerchr10:41708736..41854634hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg38145899
hg19145899
hg18145899
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv747184
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550608
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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