A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044168



Internal ID19133387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112620973..112822829hg38UCSC Ensembl
Innerchr9:115383253..115585109hg19UCSC Ensembl
Innerchr9:114423074..114624930hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38201857
hg19201857
hg18201857
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7701n100
Supporting Variantsnssv3695066, nssv3695064, nssv3695065, nssv3695063
Samples
Known GenesINIP, KIAA1958, SNX30
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044168
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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