A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552051



Internal ID15992774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100904892..100984619hg38UCSC Ensembl
Innerchr10:102664649..102744376hg19UCSC Ensembl
Innerchr10:102654639..102734366hg18UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3879728
hg1979728
hg1879728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv756071
Samples
Known GenesFAM178A, MIR608, MRPL43, SEMA4G
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552051
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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