A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038974



Internal ID18781505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:77572991..77720183hg38UCSC Ensembl
Innerchr11:77284036..77431228hg19UCSC Ensembl
Innerchr11:76961684..77108876hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38147193
hg19147193
hg18147193
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1234n100
Supporting Variantsnssv3710662, nssv3710661
Samples
Known GenesAQP11, CLNS1A, RSF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038974
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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