A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550411



Internal ID15991134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35638239..35642148hg38UCSC Ensembl
Innerchr10:35927167..35931076hg19UCSC Ensembl
Innerchr10:35967173..35971082hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg383910
hg193910
hg183910
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1036n54
Supporting Variantsnssv746845, nssv746846
Samples
Known GenesFZD8, MIR4683
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550411
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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