A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551566



Internal ID16338975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:78762880..78779103hg38UCSC Ensembl
Innerchr10:80522637..80538860hg19UCSC Ensembl
Innerchr10:80192643..80208866hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3816224
hg1916224
hg1816224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv751746
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551566
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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