A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040005



Internal ID18782536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134316739..134469090hg38UCSC Ensembl
Innerchr9:137208585..137360936hg19UCSC Ensembl
Innerchr9:136348406..136500757hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38152352
hg19152352
hg18152352
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7723n100
Supporting Variantsnssv3696429, nssv3696430
Samples
Known GenesMIR4669, RXRA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040005
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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