A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054490



Internal ID19143709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96568385..96939152hg38UCSC Ensembl
Innerchr11:96439395..96810152hg19UCSC Ensembl
Innerchr11:95944605..96315362hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38370768
hg19370758
hg18370758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3522185
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)nsv1054490
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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