A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045853



Internal ID18788384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55595852..55636296hg38UCSC Ensembl
Innerchr11:55363328..55403772hg19UCSC Ensembl
Innerchr11:55119904..55160348hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3840445
hg1940445
hg1840445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1175n100
Supporting Variantsnssv3517515
Samples
Known GenesOR4C11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045853
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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