A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552207



Internal ID16339616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:115469284..115565116hg38UCSC Ensembl
Innerchr10:117228794..117324626hg19UCSC Ensembl
Innerchr10:117218784..117314616hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3895833
hg1995833
hg1895833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1400n54
Supporting Variantsnssv758789
Samples
Known GenesATRNL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552207
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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