A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040923



Internal ID19130142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125981818..126025209hg38UCSC Ensembl
Innerchr9:128744097..128787488hg19UCSC Ensembl
Innerchr9:127783918..127827309hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3843392
hg1943392
hg1843392
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7715n100
Supporting Variantsnssv3695232
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)nsv1040923
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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