A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551799



Internal ID16339208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86942473..86943134hg38UCSC Ensembl
Innerchr10:88702230..88702891hg19UCSC Ensembl
Innerchr10:88692210..88692871hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38662
hg19662
hg18662
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1327n54
Supporting Variantsnssv752241, nssv752240
Samples
Known GenesMMRN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551799
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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