A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551435



Internal ID16338844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68642219..68796440hg38UCSC Ensembl
Innerchr10:70401976..70556197hg19UCSC Ensembl
Innerchr10:70071982..70226203hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38154222
hg19154222
hg18154222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv749986
Samples
Known GenesCCAR1, SNORD98, TET1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551435
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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