A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550324



Internal ID15991047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:29681323..29711470hg38UCSC Ensembl
Innerchr10:29970252..30000399hg19UCSC Ensembl
Innerchr10:30010258..30040405hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3830148
hg1930148
hg1830148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv745713
Samples
Known GenesSVIL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550324
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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