A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051231



Internal ID18793762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134261330..134467038hg38UCSC Ensembl
Innerchr9:137153176..137358884hg19UCSC Ensembl
Innerchr9:136292997..136498705hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38205709
hg19205709
hg18205709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7722n100
Supporting Variantsnssv3696419
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)nsv1051231
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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