A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054560



Internal ID19143779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90124374..90166359hg38UCSC Ensembl
Innerchr11:89857542..89899527hg19UCSC Ensembl
Innerchr11:89497190..89539175hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3841986
hg1941986
hg1841986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3522665
Samples
Known GenesNAALAD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054560
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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