A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174588



Internal ID15509069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1242546..1333474hg38UCSC Ensembl
Innerchr11:1263776..1354704hg19UCSC Ensembl
Innerchr11:1220352..1311280hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3890929
hg1990929
hg1890929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552927
Supporting Variants
Samples1782681313_A
Known GenesMIR6744, MUC5B, TOLLIP, TOLLIP-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174588
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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