A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047985



Internal ID18790516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67708130..67979689hg38UCSC Ensembl
Innerchr11:67475601..67747160hg19UCSC Ensembl
Innerchr11:67232177..67503736hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38271560
hg19271560
hg18271560
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1215n100
Supporting Variantsnssv3514506
Samples
Known GenesFAM86C2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047985
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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