A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029665



Internal ID18772196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5687332..6775107hg38UCSC Ensembl
Innerchr9:5687332..6775107hg19UCSC Ensembl
Innerchr9:5677332..6765107hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381087776
hg191087776
hg181087776
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3758100
Samples
Known GenesERMP1, GLDC, IL33, KDM4C, KIAA1432, KIAA2026, MIR4665, MLANA, RANBP6, TPD52L3, UHRF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029665
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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