A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549783



Internal ID15990506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1238725..1240333hg38UCSC Ensembl
Innerchr10:1281754..1282372hg19UCSC Ensembl
Innerchr10:1271754..1272372hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg381609
hg19619
hg18619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv930n54
Supporting Variantsnssv740207
Samples
Known GenesADARB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549783
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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