A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041229



Internal ID19130448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97697669..97779916hg38UCSC Ensembl
Innerchr11:97568669..97650916hg19UCSC Ensembl
Innerchr11:97073879..97156126hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3882248
hg1982248
hg1882248
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3511001
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)nsv1041229
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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