A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549797



Internal ID15990520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1693855..1714448hg38UCSC Ensembl
Innerchr10:1736049..1756642hg19UCSC Ensembl
Innerchr10:1726049..1746642hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3820594
hg1920594
hg1820594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv740231
Samples
Known GenesADARB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549797
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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