A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053482



Internal ID18796013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4116832..4254903hg38UCSC Ensembl
Innerchr11:4138062..4276133hg19UCSC Ensembl
Innerchr11:4094638..4232709hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38138072
hg19138072
hg18138072
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3522504
Samples
Known GenesLOC100506082, RRM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053482
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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