A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045123



Internal ID18787654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:133926415..133959811hg38UCSC Ensembl
Innerchr11:133796310..133829706hg19UCSC Ensembl
Innerchr11:133301520..133334916hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3833397
hg1933397
hg1833397
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1301n100
Supporting Variantsnssv3507940
Samples
Known GenesIGSF9B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045123
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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