A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1633n100



Internal ID20153249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40217600..40371437hg38UCSC Ensembl
chr13:40791737..40945574hg19UCSC Ensembl
chr13:39689737..39843574hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38153838
hg19153838
hg18153838
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046983, nsv1039012
Samples
Known GenesLINC00548, LINC00598
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1633n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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