A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038170



Internal ID18780701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134290405..134450961hg38UCSC Ensembl
Innerchr9:137182251..137342807hg19UCSC Ensembl
Innerchr9:136322072..136482628hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38160557
hg19160557
hg18160557
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7722n100
Supporting Variantsnssv3696423
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)nsv1038170
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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