A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046658



Internal ID18789189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:108687608..108841186hg38UCSC Ensembl
Innerchr9:111449888..111603466hg19UCSC Ensembl
Innerchr9:110489709..110643287hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38153579
hg19153579
hg18153579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697651
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046658
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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