A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551807



Internal ID16339216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86942633..86943134hg38UCSC Ensembl
Innerchr10:88702390..88702891hg19UCSC Ensembl
Innerchr10:88692370..88692871hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38502
hg19502
hg18502
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1327n54
Supporting Variantsnssv752254, nssv752252, nssv752253
Samples
Known GenesMMRN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551807
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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