A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045858



Internal ID18788389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:58780299..58907095hg38UCSC Ensembl
Innerchr11:58547772..58674568hg19UCSC Ensembl
Innerchr11:58304348..58431144hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38126797
hg19126797
hg18126797
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1207n100
Supporting Variantsnssv3509829, nssv3514310, nssv3509862
Samples
Known GenesGLYATL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045858
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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