A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042139



Internal ID18784670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:44691379..44893797hg38UCSC Ensembl
Innerchr11:44712929..44915348hg19UCSC Ensembl
Innerchr11:44669505..44871924hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38202419
hg19202420
hg18202420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710119
Samples
Known GenesTSPAN18
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042139
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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