A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551797



Internal ID16339206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86942473..86942967hg38UCSC Ensembl
Innerchr10:88702230..88702724hg19UCSC Ensembl
Innerchr10:88692210..88692704hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38495
hg19495
hg18495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1325n54
Supporting Variantsnssv752238
Samples
Known GenesMMRN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551797
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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