A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549790



Internal ID15990513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1327073..1329415hg38UCSC Ensembl
Innerchr10:1369268..1371610hg19UCSC Ensembl
Innerchr10:1359268..1361610hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg382343
hg192343
hg182343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv740221
Samples
Known GenesADARB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549790
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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