A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049709



Internal ID19138928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25128545..25584298hg38UCSC Ensembl
Innerchr11:25150091..25605844hg19UCSC Ensembl
Innerchr11:25106667..25562420hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38455754
hg19455754
hg18455754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3512166
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)nsv1049709
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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