A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1735n100



Internal ID22787822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:103596790..103625669hg38UCSC Ensembl
chr13:104249140..104278019hg19UCSC Ensembl
chr13:103047141..103076020hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3828880
hg1928880
hg1828880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053244, nsv1054497
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1735n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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