A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046242



Internal ID18788773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134261330..134416396hg38UCSC Ensembl
Innerchr9:137153176..137308242hg19UCSC Ensembl
Innerchr9:136292997..136448063hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38155067
hg19155067
hg18155067
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7722n100
Supporting Variantsnssv3696411, nssv3696412
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)nsv1046242
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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