A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551180



Internal ID16338589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:62206628..62290529hg38UCSC Ensembl
Innerchr10:63966387..64050288hg19UCSC Ensembl
Innerchr10:63636393..63720294hg18UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3883902
hg1983902
hg1883902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1201n54
Supporting Variantsnssv748925
Samples
Known GenesRTKN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551180
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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