A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043098



Internal ID19132317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37132330..37223487hg38UCSC Ensembl
Innerchr11:37153880..37245037hg19UCSC Ensembl
Innerchr11:37110456..37201613hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3891158
hg1991158
hg1891158
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514806
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)nsv1043098
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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