A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615141



Internal ID16402550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107051166..107077209hg38UCSC Ensembl
Innerchr9:109813447..109839490hg19UCSC Ensembl
Innerchr9:108853268..108879311hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3826044
hg1926044
hg1826044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176108
Samples1780854326_A
Known GenesMIR548Q
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615141
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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