A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552202



Internal ID16339611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:114025486..114040878hg38UCSC Ensembl
Innerchr10:115785245..115800637hg19UCSC Ensembl
Innerchr10:115775235..115790627hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3815393
hg1915393
hg1815393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv758783
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552202
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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