A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551808



Internal ID16339217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86942633..86943187hg38UCSC Ensembl
Innerchr10:88702390..88702944hg19UCSC Ensembl
Innerchr10:88692370..88692924hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38555
hg19555
hg18555
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1327n54
Supporting Variantsnssv752255
Samples
Known GenesMMRN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551808
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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