A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1613n100



Internal ID20153229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:21319810..21357467hg38UCSC Ensembl
chr13:21893949..21931606hg19UCSC Ensembl
chr13:20791949..20829606hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3837658
hg1937658
hg1837658
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035857, nsv1040997, nsv1047558
Samples
Known GenesLINC00539, MIPEPP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1613n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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