A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551780



Internal ID16339189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86366401..86367529hg38UCSC Ensembl
Innerchr10:88126158..88127286hg19UCSC Ensembl
Innerchr10:88116138..88117266hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg381129
hg191129
hg181129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1319n54
Supporting Variantsnssv752223, nssv752222
Samples
Known GenesGRID1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551780
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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