A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051034



Internal ID19140253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5761683..5787134hg38UCSC Ensembl
Innerchr11:5782913..5808364hg19UCSC Ensembl
Innerchr11:5739489..5764940hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3825452
hg1925452
hg1825452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1044n100
Supporting Variantsnssv3506322, nssv3504594, nssv3521487
Samples
Known GenesOR52N5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051034
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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