A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1599n100



Internal ID22787686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18471488..18741021hg38UCSC Ensembl
chr13:19045628..19315161hg19UCSC Ensembl
chr13:17943628..18213161hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38269534
hg19269534
hg18269534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041599, nsv1050977, nsv1052046, nsv1036748, nsv1039188, nsv1051097, nsv1048980
Samples
Known GenesLINC00417
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1599n100
Frequency
Sample Size11257
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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