A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016898



Internal ID19106115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11868796..12273191hg38UCSC Ensembl
Innerchr9:11868796..12273191hg19UCSC Ensembl
Innerchr9:11858796..12263191hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38404396
hg19404396
hg18404396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7426n100
Supporting Variantsnssv3689333
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)nsv1016898
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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