A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035329



Internal ID18777860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4217176..4367675hg38UCSC Ensembl
Innerchr11:4238406..4388905hg19UCSC Ensembl
Innerchr11:4194982..4345481hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38150500
hg19150500
hg18150500
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1022n100
Supporting Variantsnssv3511681, nssv3519506
Samples
Known GenesOR52B4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035329
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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