A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549793



Internal ID15990516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1558140..1558818hg38UCSC Ensembl
Innerchr10:1600335..1601013hg19UCSC Ensembl
Innerchr10:1590335..1591013hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38679
hg19679
hg18679
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv931n54
Supporting Variantsnssv740224, nssv740223
Samples
Known GenesADARB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549793
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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