A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047179



Internal ID19136398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4928726..4952787hg38UCSC Ensembl
Innerchr11:4949956..4974017hg19UCSC Ensembl
Innerchr11:4906532..4930593hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3824062
hg1924062
hg1824062
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1027n100
Supporting Variantsnssv3516951
Samples
Known GenesOR51A4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047179
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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