A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049029



Internal ID18791560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134280934..134450961hg38UCSC Ensembl
Innerchr9:137172780..137342807hg19UCSC Ensembl
Innerchr9:136312601..136482628hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38170028
hg19170028
hg18170028
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7722n100
Supporting Variantsnssv3696422, nssv3696420, nssv3696421
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)nsv1049029
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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