A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549778



Internal ID15990501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1237993..1239650hg38UCSC Ensembl
Innerchr10:1281597..1282170hg19UCSC Ensembl
Innerchr10:1271597..1272170hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg381658
hg19574
hg18574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv928n54
Supporting Variantsnssv740192
Samples
Known GenesADARB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549778
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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