A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550410



Internal ID15991133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35638239..35641744hg38UCSC Ensembl
Innerchr10:35927167..35930672hg19UCSC Ensembl
Innerchr10:35967173..35970678hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg383506
hg193506
hg183506
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1036n54
Supporting Variantsnssv746844
Samples
Known GenesFZD8, MIR4683
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550410
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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