A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550290



Internal ID16337699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28371674..28375640hg38UCSC Ensembl
Innerchr10:28660603..28664569hg19UCSC Ensembl
Innerchr10:28700609..28704575hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg383967
hg193967
hg183967
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1016n54
Supporting Variantsnssv745555, nssv745556
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550290
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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