A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551805



Internal ID16339214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86942575..86943239hg38UCSC Ensembl
Innerchr10:88702332..88702996hg19UCSC Ensembl
Innerchr10:88692312..88692976hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38665
hg19665
hg18665
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1327n54
Supporting Variantsnssv752249
Samples
Known GenesMMRN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551805
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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