A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049551



Internal ID19138770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34789633..34812093hg38UCSC Ensembl
Innerchr11:34811180..34833640hg19UCSC Ensembl
Innerchr11:34767756..34790216hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3822461
hg1922461
hg1822461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3512016
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)nsv1049551
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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