A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549772



Internal ID15990495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1237571..1239357hg38UCSC Ensembl
Innerchr10:1281487..1282045hg19UCSC Ensembl
Innerchr10:1271487..1272045hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg381787
hg19559
hg18559
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv928n54
Supporting Variantsnssv740176, nssv740177
Samples
Known GenesADARB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549772
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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