A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039206



Internal ID19128425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4503208..4560920hg38UCSC Ensembl
Innerchr11:4524438..4582150hg19UCSC Ensembl
Innerchr11:4481014..4538726hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3857713
hg1957713
hg1857713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3505706
Samples
Known GenesOR52M1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039206
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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