A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039803



Internal ID18782334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131488681..131531985hg38UCSC Ensembl
Innerchr11:131358575..131401879hg19UCSC Ensembl
Innerchr11:130863785..130907089hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3843305
hg1943305
hg1843305
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1298n100
Supporting Variantsnssv3509556
Samples
Known GenesNTM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039803
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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