A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038442



Internal ID18780973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131036593..131372984hg38UCSC Ensembl
Innerchr11:130906488..131242879hg19UCSC Ensembl
Innerchr11:130411698..130748089hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38336392
hg19336392
hg18336392
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1297n100
Supporting Variantsnssv3508547
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)nsv1038442
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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