A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050270



Internal ID19139489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54741938..54941169hg38UCSC Ensembl
Innerchr11:51176562..51377342hg19UCSC Ensembl
Innerchr11:51033138..51233918hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38199232
hg19200781
hg18200781
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3519948
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050270
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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