A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551511



Internal ID15992234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72010315..72014560hg38UCSC Ensembl
Innerchr10:73770073..73774318hg19UCSC Ensembl
Innerchr10:73440079..73444324hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg384246
hg194246
hg184246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1263n54
Supporting Variantsnssv750268
Samples
Known GenesCHST3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551511
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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