A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049126



Internal ID19138345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130574295..130612763hg38UCSC Ensembl
Innerchr9:133449682..133488150hg19UCSC Ensembl
Innerchr9:132439503..132477971hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3838469
hg1938469
hg1838469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7719n100
Supporting Variantsnssv3695258
Samples
Known GenesFUBP3, LOC100272217
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049126
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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