A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018117



Internal ID19107334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42697890..42856259hg38UCSC Ensembl
Innerchr9:44114860..44273229hg19UCSC Ensembl
Innerchr9:44054856..44213225hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38158370
hg19158370
hg18158370
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7574n100
Supporting Variantsnssv3756854, nssv3693010, nssv3756856, nssv3756853, nssv3693006, nssv3693009, nssv3756857, nssv3756855, nssv3693007, nssv3693011, nssv3693008
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)nsv1018117
Frequency
Sample Size11257
Observed Gain9
Observed Loss2
Observed Complex0
Frequencyn/a


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