A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509829



Internal ID18461424
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 StatusS
Merged Variantsnsv1045858
Supporting Variants
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)nssv3509829
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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