A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551753



Internal ID15992476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84187538..84215514hg38UCSC Ensembl
Innerchr10:85947294..85975270hg19UCSC Ensembl
Innerchr10:85937274..85965250hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3827977
hg1927977
hg1827977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv752183
Samples
Known GenesCDHR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551753
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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