A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037748



Internal ID18780279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81161451..81176042hg38UCSC Ensembl
Innerchr11:80872494..80887085hg19UCSC Ensembl
Innerchr11:80550142..80564733hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3814592
hg1914592
hg1814592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504264
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)nsv1037748
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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