A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615143



Internal ID16402552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:108243458..108270031hg38UCSC Ensembl
Innerchr9:111005738..111032311hg19UCSC Ensembl
Innerchr9:110045559..110072132hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3826574
hg1926574
hg1826574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176110
Samples1780854491_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615143
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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