A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550287



Internal ID16337696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28369346..28375869hg38UCSC Ensembl
Innerchr10:28658275..28664798hg19UCSC Ensembl
Innerchr10:28698281..28704804hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg386524
hg196524
hg186524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1015n54
Supporting Variantsnssv745552, nssv745551, nssv745550
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550287
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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