A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036721



Internal ID19125940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:98859756..98920719hg38UCSC Ensembl
Innerchr11:98730486..98791449hg19UCSC Ensembl
Innerchr11:98235696..98296659hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3860964
hg1960964
hg1860964
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3505410
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)nsv1036721
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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