A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041449



Internal ID19130668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:91037068..91142020hg38UCSC Ensembl
Innerchr11:90770236..90875188hg19UCSC Ensembl
Innerchr11:90409884..90514836hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38104953
hg19104953
hg18104953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1252n100
Supporting Variantsnssv3710702
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)nsv1041449
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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