A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036099



Internal ID18778630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131643993..131718467hg38UCSC Ensembl
Innerchr11:131513887..131588361hg19UCSC Ensembl
Innerchr11:131019097..131093571hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3874475
hg1974475
hg1874475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503340
Samples
Known GenesNTM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036099
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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