A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551647



Internal ID16339056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:81118732..81157354hg38UCSC Ensembl
Innerchr10:82878488..82917110hg19UCSC Ensembl
Innerchr10:82868468..82907090hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3838623
hg1938623
hg1838623
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv751865
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551647
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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