A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039105



Internal ID19128324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:62356434..62404820hg38UCSC Ensembl
Innerchr11:62123906..62172292hg19UCSC Ensembl
Innerchr11:61880482..61928868hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3848387
hg1948387
hg1848387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3507067
Samples
Known GenesASRGL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039105
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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