A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174628



Internal ID15855306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38230635..38292703hg38UCSC Ensembl
Innerchr11:38252185..38314253hg19UCSC Ensembl
Innerchr11:38208761..38270829hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3862069
hg1962069
hg1862069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554041
Supporting Variants
Samples1780862547_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174628
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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