A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549789



Internal ID15990512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1327073..1327546hg38UCSC Ensembl
Innerchr10:1369268..1369741hg19UCSC Ensembl
Innerchr10:1359268..1359741hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38474
hg19474
hg18474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv740219, nssv740218, nssv740220
Samples
Known GenesADARB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549789
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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