A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035068



Internal ID19124287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29897306..29934465hg38UCSC Ensembl
Innerchr9:29897304..29934463hg19UCSC Ensembl
Innerchr9:29887304..29924463hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3837160
hg1937160
hg1837160
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7500n100
Supporting Variantsnssv3755905
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)nsv1035068
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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